Nicotinamide adenine dinucleotide gene encoding fluorescent probe, preparation method therefor and application thereof

ABSTRACT

The invention relates to a genetically encoded fluorescent sensor for nicotinamide adenine dinucleotide, as well as methods of preparation and uses thereof. In one aspect, this invention relates to a sensor for detecting nicotinamide adenine dinucleotide, particularly, a recombinant fluorescent fusion protein sensor for detecting nicotinamide adenine dinucleotide. In one specific aspect, this invention relates to a recombinant fluorescent fusion protein sensor for detecting reduced nicotinamide adenine dinucleotide (NADH); in another specific aspect, this invention relates to a recombinant fluorescent fusion protein sensor for detecting oxidized nicotinamide adenine dinucleotide (NAD + ); in yet another aspect, the invention relates to a recombinant fluorescent fusion protein sensor for detecting the ratio of reduced to oxidized nicotinamide adenine dinucleotide. This invention also relates to the method of preparing the sensors, and uses of the sensors in detecting NADH, NAD + , NADH/NAD +  ratio, screening drugs and measuring NADH metabolism.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is the U.S. National Stage of PCT/CN2012/081977, filed Sep. 26, 2012, which claims the priority benefit of Chinese Application No. 201110288807.6, filed Sep. 26, 2011, incorporated by reference in their entireties herein.

FIELD OF INVENTION

The invention relates to a sensor for detecting nicotinamide adenine dinucleotide, especially, relates to a recombinant fluorescent fusion protein sensor for detecting nicotinamide adenine dinucleotide. In one specific aspect, this invention relates to a recombinant fluorescent fusion protein sensor for detecting reduced nicotinamide adenine dinucleotide (NADH); in another specific aspect, this invention relates to a recombinant fluorescent fusion protein sensor for detecting oxidized nicotinamide adenine dinucleotide (NAD⁺); in another aspect, the invention further relates to a recombinant fluorescent fusion protein sensor for detecting the ratio of reduced to oxidized nicotinamide adenine dinucleotide. This invention also relates to a process for preparing the sensors, and uses of the sensors in detecting NADH, NAD⁺ and NADH/NAD⁺ ratio.

BACKGROUND OF INVENTION

As coenzymes, NAD⁺ and NADH are important components of the respiratory chain, and involved in the electron transfer process in the respiratory chain (Rich, P. R. et al., Biochem Soc Trans. 2003, V.31 (6), pp. 1095-1105). In redox reactions of the respiratory chain, NAD⁺ acts as a proton carrier and transforms from its initial oxidation state to reduction state upon reception of an electron from other molecules; NADH, the product of this transformation, can act as a reducing agent providing electron for other molecules (Belenky. P. et al., Trends in Biochemical Sciences. 2007, V.32 (1), pp. 12-19). Recent studies have shown that, NAD(H) is not only involved in energy metabolism, substance synthesis, and antioxidation, but also relates to, inter alia, in vivo calcium homeostasis, gene expression, immunization, cell ageing and death, wherein NAD(H) plays vital roles. Accordingly, NAD(H) itself and numerous enzymes relating to NAD(H) metabolism have become targets for drug design (Sauve, A. A. et al., J Pharmacol Exp Ther. 2008, V.324(3), pp. 883-893).

However, in most living cells, the total amount of NAD(H) is about 10⁻⁶ M˜10⁻³ M, while the NAD⁺/NADH ratio also varies depending on intracellular states (Lin, S. J. et al., Current Opinion in Cell Biology. 2003, V.15(2), pp. 241-246), therefore, it is difficult to determine NAD(H). Earlier detecting methods mainly utilize the characteristic UV absorption of NADH at 340 nm, which leads to the UV spectrophotometry assay. This method has two main flaws: 1, the effective sensitivity is about 10⁻⁷ M, limited by the instrument precision; 2, effective differentiation between NADH and NADPH is not possible in complicated systems. A series of enzymatic assay are later developed based on the characteristic of NAD⁺ as a coenzyme which accepts an electron during electron transport and transforms to NADH. Other methods, such as HPLC analysis, the electrochemical assay, capillary electrophoresis, fluorescence imaging, etc., are also commonly reported in literatures. However, most of the methods either lack sensitivity towards target molecules in individual cells or lack capacity for localization to subcellular organelles. It is noteworthy that, a major common defect in these available methods is the need of sample processing including lysis, separation, and purification. As NADH itself is prone to oxidization, and errors are readily introduced, the cumbersome operations would lead to experimental results deviated from the bona fide values. In addition, these existing methods can not be applied to living animals or cells and can not detect in real time, which limits the applications in clinical diagnosis and prodrugs research. At present, NADH detection in living animals or cells can only be achieved by using NADH autofluorescence (Zhang, Q. H. et al., Science. 2002, V.295 (5561), pp. 1895-1897), but this traditional method has serious flaws as follows: first, it is known that the regulations of NAD⁺/NADH and NADP⁺/NADPH in cells are relatively independent, normally, NAD⁺/NADH ratio is about 700:1, while NADP⁺/NADPH ratio is about 1:200; second, the vast different in redox potential between NADH and NADPH indicates the distinct roles in energy metabolism and anabolism played by them; third, with NADH and NADPH autofluorescence being completely indistinguishable, the result obtained through autofluorescence imaging measurement is the sum of NADH and NADPH, and the data essentially indicates the concentration of protein-bound NADPH instead because the content of NADPH is low and mostly presented in protein binding form (Zhang, Q. H. et al., Science. 2002, V.295 (5561), pp. 1895-1897); fourth, since NADH is excited with wavelength in the ultraviolet range (340 nm) and its autofluorescence is weak, sophisticated and expensive equipments such as CritiView for clinical monitoring are required; furthermore, UV light has a rather weak capability of penetrating through tissues and can cause cell damages, so these optical properties severely restrict the application of autofluorescence monitoring.

Therefore, there is an urgent need in the art to develop a specific NADH detecting technique, especially, a specific technique which is suitable for detecting NADH in physiological level and subcellular level.

Relative to traditional detection techniques involving small molecule dye and rapid developing detection techniques using quantom dot, fluorescent protein detection technique has a unique overwhelming advantage in the imaging of most living cells; fluorescent protein can be genetically introduced into cells, tissues, and even whole organs, therefore it can be used as a whole-cell marker or gene activation indicator.

Green fluorescent protein is originally isolated from Aequorea victoria, and the wild-type AvGFP is consisted of 238 amino acids and has a molecular weight of about 26 kD. Recent study confirms that, in native GFP protein, three amino acids from 65 to 67, Ser-Tyr-Gly, are able to spontaneously form a fluorescent chromogenic moiety, wherein p-hydroxy-benzylidene-imidazolinone is the main luminous feature. The wild-type AvGFP has rather complex spectral characteristics with its main fluorescent excitation peak at 395 nm, and a secondary peak at 475 nm, whose amplitude intensity is approximately ⅓ of the main peak. Under standard solution condition, 395 nm excitation can produce 508 nm emission, and 475 nm excitation produces maximal emission at 503 nm (Heim, R. et al., Proc Natl Acad Sci USA. 1994, V.91 (26), pp. 12501-12504).

Upon intensive studies on GFP protein mutations, a variety of prominent GFP derivatives have been developed using molecular biotechnology. Through various single-point mutations or combination thereof made to the wild-type GFP, mutants such as enhanced-type GFP (S65T, F64L), YFP (T203Y) and CFP (Y66W) can be obtained. By rearranging GFP protein sequence to shift the original amino acids 145-238 to the N terminal and the amino acids 1-144 to the C terminal of the new protein, and binding the two fragments through a flexible short peptide chain, a space sensitive circular permutation fluorescent protein is formed thereby, and a T203Y point mutation thereupon results in a circular permutation yellow fluorescent protein cpYFP (Nagai, T. et al., Proc Natl Acad Sci U.S.A. 2001, V.98 (6), pp. 3197-3202).

Fluorescence-based analytical techniques have further developed along with the progression in fluorescent protein studies. One example is fluorescent resonance energy transfer (FRET) technique that is routinely adopted nowadays, the key mechanism of which is, when two fluorophores are in sufficiently close proximity, a donor entity absorbs photon of suitable frequency and is excited to a higher energy state returns to the ground state upon transferring energy to nearby acceptor entity via dipole-dipole interaction (that is, the occurrence of resonance energy transfer). FRET is a non-radiation energy transfer through intermolecular dipole-dipole interaction transferring energy from donor in excited state to result in acceptor in excited state, so that the fluorescence intensity of the donor decreases while the acceptor may emit characteristic fluorescence (sensitized fluorescence) which is stronger than its basic fluorescence, or it may emit no fluorescence (fluorescence quenching). Further studies of the green fluorescent protein show that cyan fluorescent protein (CFP) and yellow fluorescent protein (YFP) derived from green fluorescent protein mutants constitute a prominent donor/acceptor pair. Emission spectrum of CFP substantially overlaps absorption spectrum of YFP, when CFP and YFP are in sufficiently close proximity and upon the excitation with the absorption wavelength of CFP, the chromophore of CFP will effectively resonance transfer energy to the chromophore of YFP, so CFP emitted fluorescence will be weakened or disappeared, and the main emission is YFP fluorescence. The efficiency of energy transfer between the two chromophores is inversely proportional to sixth power of the spatial distance between them, and is very sensitive to changes in spatial position. Therefore, existing studies report the use of genetically engineering recombinant methods for expression of a novel fusion protein having both termini of the protein of interest fused with CFP and YFP, respectively, such that spatial change caused by binding of the protein with its specific target molecule will be visualized by the fluorescent change.

So the fluorescent protein sequence used herein may come from Aequorea victoria fluorescent protein and its derivatives, including, but not limited to sequences of the following mutants: yellow fluorescent protein (YFP), green fluorescent protein (GFP), cyan fluorescent protein (CFP), and the likes, the sequence of yellow fluorescent protein YFP is preferable, and the sequence of circular permutation yellow fluorescent protein cpYFP is particularly preferable.

The technique described herein involves another protein, YdiH protein (also known as Rex protein), a bacterial transcriptional repressor protein already known in the art, which has a molecular weight of 23 kDa and can regulate fermentation and anaerobic respiration. Generally, YdiH proteins are derived from Thermus aquaticus (SEQ ID NO: 1 NCBI GenBank: AF061257.1), Streptomyces coelicolor (SEQ ID NO: 2 NCBI GenBank: AL9391.1) or Bacillus subtilis (SEQ ID NO: 3 NCBI GenBank: AL009126.3). YdiH protein is initially identified in 2003 from Streptomyces coelicolor by Brekasis and Paget et al., which is a redox-sensitive regulatory protein that widely presents in Gram-positive bacteria. The study on YdiH (Rex) protein of Streptomyces coelicolor indicates that it is a typical NAD(H) binding protein with Rossmann domain. The key Rossmann domain is a super-secondary protein structure mainly exists in nucleotide binding proteins, and it is a typical cofactor NAD(H) binding domain, represented by various cofactor NAD(H) binding proteins. The structure is essentially comprised of 6 β-pleated sheets linked through two pairs of α-helixes in the form of β-α-β-α-β. Since each Rossmann domain can bind one nucleotide molecule only, there are two Rossmann segments presented pairwise in dinucleotide binding proteins such as these for NAD. Current studies have shown that the Streptomyces coelicolor YdiH (Rex) protein can directly probe changes in cytoplasmic NADH/NAD⁺ ratio, while under aerobic conditions, the YdiH (Rex) protein can inhibit the transcription of its target genes (cydABC, nuoA-D and rexhemACD) when intracellular NADH/NAD⁺ ratio is at low level, but dissociates from its operon region at elevated NADH/NAD⁺ ratio, and during this dynamic process, the steric configuration of YdiH (Rex) protein transforms upon environmental change (Brekasis, D. et al., EMBO J., 2003, V.22 (18), pp. 4856-4865). Therefore, Rex protein is a good candidate for intracellular NADH sensor. Meanwhile, Wang et al. recently crystallized the Bacillus subtilis YdiH (Rex) protein and investigated its mechanism and function. Their results show that YdiH(Rex) protein from Bacillus subtilis is a homodimer protein having two functional domains, wherein the N-terminal domain (residues 1-85) is a DNA-binding domain, while the C-terminal domain (residues 86-215) is a typical Rossmann fold that can bind NADH (Wang, E. et al., Mol Microbiol 2008, V.69 (2), pp. 466-4′78).

Although YdiH (Rex) protein per se is sensitive to the redox state of the environment, the changes thereof are not intuitively exhibited and can not be captured externally. While by means of the fluorescent protein, we can ideally obtain a novel genetically encoded fluorescent sensor by fusioned expression of YdiH (Rex) and fluorescent protein, YdiH (Rex) is utilized for probing environmental redox state change and relaying the change to the fluorescent protein, which will visualize the change in environmental redox state in real-time and intuitively by the presence/absence or the intensity of the fluorescence generated thereby.

In summary, we believe that the use of recombinant fluorescent fusing protein which contains YdiH protein is able to meet the urgent need to detect NADH in physiological level and subcellular level.

The citation or discussion of any reference in this specification should not be construed as an admission that such reference is available as “Prior Art” to the present invention.

SUMMARY OF INVENTION

On one aspect, this invention provides a genetically encoded fluorescent sensor for NADH, comprising a polypeptide which is sensitive to environmental NADH, and a segment that exhibits the environmental NADH by change in its spectral characteristics. In one embodiment, the segment that exhibits the environmental NADH by change in the spectral characteristic is a fluorescent protein sequence or a derivative thereof. In another embodiment, the NADH-sensitive polypeptide is a polypeptide or its functional fragment or NADH binding domains having following characteristics:

(1) comprising Rossman domain with NADH binding feature; and/or

(2) derived from an NADH sensitive protein of transcription regulatory factor Rex family.

In a preferred embodiment, the polypeptide sensitive to NADH described herein may have following characteristics:

(1) containing polypeptide derived from bacterial transcription factor Rex protein gene ydiH, wherein the polypeptide may be encoded by a sequence selected from SEQ ID NO: 1, 2 or 3;

(2) a homologous or non-homologous sequence that is 95% identical to the sequence describe in (1) in at least 85 amino acid residues;

(3) any homologous or non-homologous sequence that is 90% identical to the sequence describe in (1) in at least 85 amino acid residues;

(4) any homologous or non-homologous sequence that is 70% identical to the sequence describe in (1) in at least 85 amino acid residues;

(5) any homologous or non-homologous sequence that is 50% identical to the sequence describe in (1) in at least 85 amino acid residues;

(6) any homologous or non-homologous sequence that is 40% identical to the sequence describe in (1) in at least 85 amino acid residues; or

(7) any homologous or non-homologous sequence that is 35% identical to the sequence describe in (1) in at least 85 amino acid residues.

In another embodiment, the fluorescent sensor of this invention may contain Rossman domain B characterized by NADH binding property and fluorescent protein sequence A, A1 and/or A2, which may be combined in a form of:

(1) B-A-B;

(2) B-A-B-B;

(3) A1-B-A2, wherein A1 and A2 can be identical or different; A1 can be an amino acid sequence derived from Aequorea Victoria fluorescent protein or a derivative thereof, and A2 can be an amino acid sequence derived from another Aequorea victoria fluorescent protein or a derivative thereof;

(4) a first portion of B-A-a second portion of B; wherein A is inserted in the flexible region of B such that B is segmented into the first portion and the second portion, while the first portion of B and the second portion of B constitute a complete B domain; or

(5) a first portion of B-A-a second portion of B-B; wherein A is inserted in the flexible region of B such that B is segmented into the first portion and the second portion of B, while the first portion of B and the second portion of B constitute a complete B domain.

In yet another embodiment, the fluorescent sensor in this invention may also have the following structure:

A₁-B₁-Linker₁-FM-Linker₂-B₂,

wherein A₁ is a first domain of YdiH protein, preferably containing amino acids 1-84 of Bacillus subtilis YdiH protein sequence (SEQ ID NO: 14), or amino acids 1-79 of Thermus aquaticus YdiH protein sequence (SEQ ID NO: 15), or variant thereof; B₁ is a second domain of YdiH protein, preferably containing amino acids 85-194 of Bacillus subtilis YdiH protein sequence (SEQ ID NO: 16), or amino acids 80-189 of Thermus aquaticus YdiH protein sequence (SEQ ID NO: 17), or variant thereof; B₂ is a third domain of YdiH protein, preferably containing amino acids 120-215 of Bacillus subtilis YdiH protein sequence (SEQ ID NO: 18), or amino acids 114-211 of Thermus aquaticus YdiH protein sequence (SEQ ID NO: 19), or variant thereof;

FM is a fluorophore, and it can be YFP, GFP, CFP and variants derived from these proteins, wherein YFP is preferable, and cpYFP is more preferable;

Linker₁ may be present or absent; if present, Linker₁ can be any amino acid sequence, preferably not longer than 4 amino acids, for example, it may contain amino acids T, S, A, G, or may be any combination of any 1 to 4 amino acids of them, e.g., amino acid sequence SAG or TS or the likes, but not limited thereto;

Linker₂ may be present or absent; if present, Linker₂ can be any amino acid sequence, preferably not longer than 3 amino acids, for example, it may contain amino acids G, T, G, or may be any combination of any 1 to 3 amino acids of them, e.g., amino acid sequence GTG, but not limited thereto.

In one embodiment, this invention also provides a fluorescent sensor containing a fluorophore, and a YdiH protein or any one of protein fragments, derivatives or analogs of YdiH. In another embodiment, the invention also provides a fluorescent sensor containing a fluorophore and a YdiH protein variant. The invention also provides a fluorescent sensor containing a fluorophore and a soluble fragment of YdiH protein.

In one embodiment, this invention provides a fluorescent sensor comprising the amino acid sequence of SEQ ID NO: 4, 5, 6, 7 or 8. In a preferred embodiment, this invention provides a fluorescent sensor comprising a homologous and non-homologous sequence having 99%, 95%, 90%, 80%, 70% or 50% identity with amino acid sequence SEQ ID NO: 4, 5, 6, 7 or 8 in at least 85 amino acid residues. In a preferred embodiment, this invention provides a fluorescent sensor comprising a homologous or non-homologous sequence that is substantially similar or identical to amino acid sequence SEQ ID NO: 4, 5, 6, 7 or 8 in at least 85 amino acid residues. In a preferred embodiment, this invention provides a fluorescent sensor comprising a mutant or derivative of amino acid sequence SEQ ID NO: 4, 5, 6, 7 or 8.

In another embodiment, the invention also provides a genetically encoded fluorescent sensor for NAD⁺, comprising a polypeptide which is sensitive to environmental NAD⁺, and a segment that exhibits the environmental NAD⁺ by change in its spectral characteristics. In a specific embodiment, the fluorescent sensor for NAD⁺ comprises SEQ ID NO: 129.

In another embodiment, the invention also provides a genetically encoded fluorescent sensor for NADH/NAD⁺ ratio, comprising a polypeptide sensitive to environmental NADH/NAD⁺ ratio, and a segment that exhibits the environmental NADH/NAD⁺ ratio by change in its spectral characteristics. In a specific embodiment, the fluorescent sensor for NADH/NAD⁺ ratio comprises SEQ ID NO: 148.

In another aspect, the invention provides a fusion protein comprising the fluorescent sensor of this invention. In one embodiment, the fusion protein comprises the fluorescent sensor of this invention and various specific signal for subcellular localization, wherein the signal allows localization of a target protein into a specified subcellular organelle.

In another aspect, the invention provides a nucleic acid sequence comprising the nucleotide sequence that encodes the fluorescent sensor or the fusion protein of the invention. In a specific embodiment, the invention provides a nucleic acid sequence comprising the nucleotide sequence encoding a fluorescent protein and a nucleotide sequence encoding a NADH sensitive protein.

In a preferred embodiment, the nucleotide sequence encoding the NADH sensitive protein is a nucleotide sequence encoding a polypeptide or its functional fragments or NADH binding domain having following characteristics:

(1) comprising a Rossman domain with NADH binding feature; and/or

(2) derived from an NADH sensitive protein of transcription factor Rex family

In another preferred embodiment, the nucleic acid sequence of the invention may comprise a coding sequence b for a Rossman domain having NADH binding feature and coding sequences a, a1 and/or a2 for fluorescent protein(s), in an arrangement of the following:

(1) b-a-b;

(2) b-a-b-b;

(3) a1-b-a2, wherein a1 and a2 can be the identical or not; a1 can be a coding sequence of a fluorescent protein from Aequorea victoria or a derivative thereof, a2 can be a coding sequence of another fluorescent protein from Aequorea victoria or a derivative thereof;

(4) a first portion of b-a-a second portion of b; wherein a is inserted in the flexible region of b such that b is segmented into the first portion of b and the second portion of b, while the first portion of b and the second portion of b constitute a complete b domain;

(5) a first portion of b-a-a second portion of b-b; wherein a is inserted in the flexible region of b such that b is divided into the first portion of b and the second portion of b, while the first portion of b and the second portion of b constitute a complete b domain.

In another preferred embodiment, the invention provides a nucleic acid sequence comprising nucleotide sequence SEQ ID NO: 9, 10, 11, 12, or 13. In a preferred embodiment, the invention provides a nucleic acid sequence comprising any homologous and non-homologous sequences having 99%, 95%, 90%, 80%, 70% or 50% identity with the nucleotide sequence SEQ ID NO: 9, 10, 11, 12 or 13 in at least 85 bases in length. In another preferred embodiment, the invention provides a nucleic acid sequence comprising nucleotide sequence that is substantially similar or identical to the nucleotide sequence of SEQ ID NO: 9, 10, 11, 12 or 13 in at least 85 bases; in a preferred embodiment, the invention provides a nucleic acid sequence comprising a variant or derivative of the nucleotide sequence of SEQ ID NO: 9, 10, 11, 12 or 13.

The present invention also relates to a complementary sequence and a variant of the aforementioned nucleic acid sequence, which may include a nucleic acid sequence or a complement of the sequences encoding fragments, analogues, derivatives, soluble fragments and variants of the fluorescent sensor or fusion protein of the invention.

In yet another aspect, the invention also provides an expression vector comprising the nucleic acid sequence of the invention operably linked to a expression control sequence. The expression control sequence can be an origin of replication, a promoter, an enhancer, an operon, a terminator, or a ribosome binding sites, etc.

In yet another aspect, the present invention also provides a host cell containing the expression vector of the invention.

In yet another aspect, the present invention also provides a method for preparing the fluorescent sensor or the fusion protein of this invention, comprising the following steps:

a. transferring the expression vector of the invention into a host cell,

b. culturing the host cell under conditions suitable for the expression in the host cell, and

c. separating the fluorescent sensor or fusion protein from host cells.

The invention also provides uses of the fluorescent sensor or the fusion protein of the invention in detecting NADH. In one embodiment, the invention provides uses of the fluorescent sensor or the fusion protein of the invention in detecting NADH in vitro or in vivo. In one embodiment, the invention provides uses of the fluorescent sensor or the fusion protein of the invention in detecting NADH at subcellular level. In one embodiment, the invention provides uses of the fluorescent sensor or the fusion protein in detecting NADH in situ. In another embodiment, the invention provides uses of the fluorescent sensor or the fusion protein of the invention in drug screening, wherein the drugs may be used to adjust NADH level in a subject. In another embodiment, the invention provides uses of the fluorescent sensor or the fusion protein of the invention in diagnosis of diseases which are associated with the level of NADH.

The invention also provides a kit for NADH detection, which comprises the fluorescent sensor or the fusion protein of the invention. The detection can be conducted in vitro, in vivo, in situ, or at subcellular level. The invention also provides a kit for screening drug which can be used to adjust the NADH level in a subject, wherein the kit comprises an effective amount of fluorescent sensor or fusion protein of the invention. The invention also provides a kit for diagnosing diseases associated with the level of NADH, wherein the kit comprises an effective amount of the fusion protein of the invention. For said uses, one skilled in the art can readily determine the effective amount based on the activity of the fusion protein of the invention.

The protein and nucleic acid sequences of the invention are preferably provided in isolated form, and more preferably purified to homogeneity.

BRIEF DESCRIPTION OF THE FIGURES

The invention is further described with reference to the following figures and examples.

FIG. 1 shows SDS-PAGE characterizing F-rex1 separated and purified from E. coli.

FIG. 2 shows SDS-PAGE characterizing F-rex2 separated and purified from E. coli.

FIG. 3 shows basic spectral characteristics of the nicotinamide adenine dinucleotide fluorescent sensor F-rex1.

FIG. 4 shows basic spectral characteristics of the nicotinamide adenine dinucleotide fluorescent sensor F-rex2.

FIG. 5 shows response of fluorescent sensor F-rex1 for reduced nicotinamide adenine dinucleotide to pyridine nucleotide analogs under simulated physiological conditions in vitro.

FIG. 6 shows response of the derivatized fluorescent sensor for reduced nicotinamide adenine dinucleotide to pyridine nucleotide analogs under simulated physiological conditions in vitro.

FIG. 7 shows changes of NADH in HEK293FT cells after the treatment of 3-NP and AOA.

FIG. 8-1 shows the real-time measurements of the NADH change within cells treated with exogenous NADH using a sensor for NADH/NAD⁺ ratio.

FIG. 8-2 shows the real-time measurements of the NADH change within cells treated with glucose, pyruvic acid, lactic acid using a sensor for NADH/NAD⁺ ratio.

FIG. 8-3 shows the real-time measurements of the NADH level change within mitochondrias using a sensor for NADH/NAD⁺ ratio.

FIG. 9-1 shows the detection of cytosolic NAD⁺ change using an NAD sensor.

FIG. 9-2 shows the change of the response of NAD⁺ sensor to NAD⁺ in vitro.

FIG. 9-3 shows the response of NAD⁺ sensor to pyridine nucleotide analogs under simulated physiological conditions in vitro.

FIG. 10-1 shows the characteristics of the sensor for NADH/NAD⁺ ratio in response to the combination of NADH and NAD⁺.

FIG. 10-2 shows the measurement results using the sensor for NADH/NAD⁺ ratio at various NADH/NAD⁺ ratios.

FIG. 10-3 shows the detection of the effect of pyridine nucleotide analogs to the sensor for NADH/NAD⁺ ratio under simulative physiological conditions in vitro.

FIG. 11 shows a high-throughput drug screening scheme based on the sensor for NADH/NAD⁺ ratio fluorescence.

FIG. 12 shows a real-time detection of the metabolite levels of NADH/NAD⁺ ratio in tumors by sensor for NADH/NAD⁺ ratio fluorescent.

DESCRIPTION OF THE EMBODIMENTS I. Definitions

When a numerical value or range is indicated, the term “about” used herein means the value or range is within 20%, 10% and 5% of the indicated value or range.

Terms such as “containing”, “comprising” and its equivalents used herein shall be read as encompasses the meaning of “having” and “consisting of . . . ”, for example, a composition “containing” X may consist exclusively of X or may include other substances, like X+Y.

In the invention, the term “YdiH protein” refers to protein YdiH (also known as Rex protein), which is a bacterial transcriptional inhibiting protein already known in the art. YdiH has a molecular weight of 23 kDa and regulates the fermentation and anaerobic respiration. It is a type of redox-sensitive regulatory protein which widely exists in Gram-positive bacteria, and is a typical NAD(H)-binding protein that containing Rossmann domain. The key Rossmann domain therein is a super secondary protein structure mainly presents in nucleotide binding proteins, a typical region active in binding cofactor NAD(H), and is represented by various cofactor NAD binding proteins. The structure is essentially comprised of 6 β-sheets linked through two pairs of α-helixes in the form of β-α-β-α-β. Since each Rossmann domain could bind one nucleotide molecule only, there are two Rossmann segments presented pairwise in dinucleotide-binding protein domains such as these for NAD. YdiH (Rex) protein can directly probe changes in cytoplasmic NADH/NAD⁺ ratio, but under aerobic conditions, YdiH (Rex) protein can inhibit transcription of its target genes (cydABC, nuoA-D and rexhemACD) when intracellular NADH/NAD⁺ ratio is at low level, while dissociates from its operon region at elevated NADH/NAD⁺ ratio, and the steric configuration of YdiH (Rex) protein transforms upon the environment changes during this dynamic process. The “YdiH protein” involved in the invention may contain amino acid sequence encoded by nucleotide sequence of SEQ ID NO: 1 or SEQ ID NO: 2 or SEQ ID NO: 3. The “flexible region” referred to in the invention means specific structure, such as Loop configuration, presents in advanced protein structure. These structures exhibit better mobility and flexibility than other advanced structures of proteins, and are capable of causing dynamic change of domains, while proteins also exhibit significant tendency of undergo spatial conformational change in such regions. The flexible region referred to in the invention mainly means the V113-G119 region and D188-G192 region of T-rex (the Rex protein from Thermus aquaticus).

The term “fluorescent sensor” used herein refers to a polypeptide sensitive to environmental NADH and fused with a fluorescent protein, specifically, the polypeptide sensitive to environmental NADH can be a YdiH protein. The sensor utilizes the conformational changes of the fluorescent protein caused by binding of the NADH-specific binding structure Rossman domain in YdiH with NADH, and thus lead to the generation or reduction of fluorescence, or changes in the generated fluorescence; plotting standard curve based on the fluorescence of fluorescent protein measured under different NADH concentrations would, in turn, allow the detection and analy the presence and/or level of NADH.

The term “fusion protein” is synonymous with the terms “fluorescent fusion protein” and “recombinant fluorescent fusion protein”, refers a polypeptide or protein comprising an amino acid sequence of a first polypeptide or protein, or fragment, analog or derivative thereof, and an amino acid sequence of a heterologous polypeptide or protein (that is, a second polypeptide or protein, or fragment, analog or derivative thereof, which differs from the first polypeptide or protein, or fragment, analog or derivative thereof). In one embodiment, the fusion protein comprises a fluorescent protein fused with the heterologous protein, polypeptide or peptide. According to this embodiment, the heterologous protein, polypeptide or peptide may or may not be a fluorescent protein of different type. In one embodiment, the fusion protein maintains or enhances its activity relative to the activity of the original polypeptide or protein prior to the fusion with heterologous protein, polypeptide or peptide. In a specific embodiment, the fusion protein comprises a fluorescent sensor fused with a heterologous protein, polypeptide or peptide, wherein the heterologous protein, polypeptide or peptide can be a specific subcellular localization signal.

The term “fluorophore” used here is synonymous with “fluorescent protein”, representing a protein exhibits autofluorescence or emits fluorescence under illumination. Fluorescent proteins are often used as detection means, for instance, green fluorescent protein GFP and BFP, CFP, YFP, etc, derived therefrom GFP are routinely used in the biotechnology arts.

The term “GFP” used herein refers to green fluorescent protein, which is originally isolated from Aequorea victoria. The wild type AvGFP is consisted of 238 amino acids and has a molecular weight of about 26 kD, and amino acid sequence SEQ ID No: 20. Recent study confirms that Ser-Tyr-Gly, the three amino acids 65-67 in native GFP protein, are able to spontaneously form a fluorescent chromophore: p-hydroxybenzylideneimidazolinone, which is the primary emitting site. The wild-type AvGFP exhibits very complex spectral characteristics with its main fluorescence excitation peak at 395 nm and a secondary peak at 475 nm, whose amplitude intensity is about ⅓ of the main peak. Under standard solution condition, 395 nm excitation can produce 508 nm emission, and 475 nm excitation produces maximum emission at 503 nm wavelength.

The term “YFP” used herein refers to yellow fluorescent protein, which is derived from green fluorescent protein GFP, the amino acid sequence of which is up to 90% or more homologous to GFP, and the key change of YFP from GFP is that the substitution of amino acid 203 from threonine to tyrosine (T203Y), Compared to original AvGFP, the main excitation peak of YFP is red-shifted to 514 nm wavelength and emission wavelength shifted to 527 nm. Site-directed mutation of amino acid no. 65 of the YFP (S65T) thereupon will obtain the fluorescence enhanced yellow fluorescent protein EYFP, and typical EYFP amino acid sequence is SEQ ID NO: 21. And sequence rearrangement of the EYFP protein by having the original amino acids 145-238 as the N terminus, and the original amino acid 1-144 as the C terminus of the new protein, with the two fragments linked through a short flexible peptide chain VDGGSGGTG (residues 312-320 of SEQ ID NO:5) forms cpYFP (circular permutation yellow fluorescent protein) that is sensitive to spacial changes, and typical cpYFP amino acid sequence is SEQ ID NO: 22.

In this invention, the YdiH protein that fused with fluorophore can be a full length native YdiH protein, or a fragment thereof, isolated from Bacillus subtilis or Thermus aquaticus or Streptomyces coelicolor; amino acids 1-215 of native YdiH protein from Bacillus subtilis or amino acids 1-211 of YdiH protein from Thermus aquaticus, or amino acids 1-259 of YdiH protein from Streptomyces coelicolor are preferable; while amino acids 1-215 of YdiH protein from Bacillus subtilis or tamino acids 1-211 of YdiH protein from Thermus aquaticus are more preferable.

“Linker” means an amino acid or nucleic acid sequence linking the two segments within a polypeptide, protein or nucleic acid in the invention. When linking for a polypeptide or protein of the invention, the length of the linker is no longer than 6 amino acids, preferably, no longer than four amino acids, more preferably, 3 amino acids. When linking for a nucleic acids of the invention, the length of the linker is no longer than 18 nucleotides, preferably no longer than 12 nucleotides, more preferably 9 nucleotides.

When referring to a polypeptide or protein, the term “variant” used herein includes variants of the polypeptide or protein with the same function but differ in sequence. These variants include, but not limited to, sequences obtained by deleting, inserting and/or substituting one or more (typically 1-30, preferably 1-20, more preferably 1-10, and most preferably 1-5) amino acid(s) in the sequence of the polypeptide or protein, and by adding one or more (usually less than 20, preferably less than 10, and more preferably within 5) amino acid(s) to its C-terminus and/or N-terminus. For example, in the art, substitution with amino acids of comparable or similar properties usually does not change the function of the polypeptide or protein. Amino acids with similar properties usually refer to a family of amino acids having similar side chains and have been clearly defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), amino acids with acidic side chains (e.g., aspartate, glutamate), amino acids with uncharged polar side chain (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), amino acids with non-polar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), amino acids with β-branched side chains (e.g., threonine, valine, isoleucine), and amino acids with aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). As another example, adding one or more amino acids to the C-terminus and/or N-terminus usually does not change the function of the polypeptide or protein either. As known to a person skilled in the art, genetic cloning process often requires design of suitable endonuclease sites, which will eventually introduce one or more irrelevant residues to the terminus of the polypeptide or protein to be expressed, but this does not affect the activity of the target polypeptide or protein. For another example, in order to construct a fusion protein, to promote the expression of a recombinant protein, to obtain a recombinant protein that can secrete itself into the extracellular environment of the host cells, or to facilitate the purification of a recombinant protein, it is often desirable to have the N-terminus, C-terminus, or other suitable regions of the protein added with some amino acids, for example, including, but not limited to, suitable connecting peptides, signal peptides, leader peptides, the terminal extensions, the glutathione S-transferase (GST), maltose E binding protein, Protein A, tags such as 6His or Flag, or factor Xa or thrombin or enterokinase protease cleavage sites. Variants of the polypeptide or protein may include: homologous sequences, conservative variants, allelic variants, natural mutants, induced mutants, polypeptide or protein encoded by a DNA which could hybridize with the DNA for said polypeptide or protein under high or low stringent conditions, as well as the polypeptide or protein derived from antiserum against said polypeptide or protein. These variants may also comprise polypeptide or protein whose sequence is at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 98%, at least about 99%, or 100% sequence identity with said polypeptide or protein.

In the context of two or more polypeptides or nucleic acid sequences, the term “identical” or “percent identity” means, when compared and aligned for maximum correspondence over a comparing window or designated region using available methods such as comparing algorithms known in the art or by manual alignment and visual inspection, two or more sequences or sub-sequences are the same or have a specified percentage of amino acid residues or nucleotides that are the same (e.g., 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% are the same). For example, preferred algorithms that are suitable for determining the percent sequence identity or similarity are the BLAST and BLAST 2.0 algorithms, which can be found in Altschul (1977) Nucleic Acids Res. 25:3389 and Altschul (1990) J. Mol. Biol. 215:403, respectively.

The term “soluble fragment” used herein generally refers to fragments having at least about 10 consecutive amino acids of the full-length protein sequence, usually at least about 30 consecutive amino acids, preferably at least about 50 consecutive amino acids, more preferably at least about 80 consecutive amino acids, and optimally at least about 100 consecutive amino acids.

The terms “functional fragment”, “derivative” and “analog” mean proteins retain substantially the same biological function or activity of the native YdiH protein in the invention. Functional fragments, derivatives or analogs of YdiH in the invention may be (i) proteins with one or more conservative or non-conservative amino acid substitution (preferably conservative), where the substituted amino acid residues may or may not be one encoded by the genetic code, or (ii) proteins containing substitutions of one or more amino acid residues having a substituent group, or (iii) proteins formed having the mature protein fused with another compound (such as compounds that extend half-life of the protein, for example, polyethylene glycol), or (iv) proteins formed by having said protein fused with additional amino acid sequence (such as leader sequence or secretory sequence, or sequence used for purification of the protein or proprotein sequence, or fusion protein formed with fragment of antigen IgG). In accordance with the teachings provided herein, these functional fragments, derivatives and analogs are well known to a person skilled in the art.

The differences between analogs and the native YdiH protein may be the difference in amino acid sequences, and may also be the difference in the forms of modifications that will not affect the sequence, or both. These proteins include natural or induced genetic variants. Induced variants can be obtained by a variety of techniques, such as generating random mutagenesis by irradiation or exposure to mutagens, and can also be obtained by directed mutagenesis or other known molecular biology techniques.

Analogs mentioned herein also include analogs with residue(s) different from natural L-amino acid (e.g., D-amino acids), as well as analogs with a non-naturally occurred or synthetic amino acid (such as β, γ-amino acids). It should be understood that the YdiH protein of the invention is not limited to the representative proteins, fragments, derivatives and analogs exemplified above. Forms of modification (usually without change of the primary structure): chemical derivatization of the protein in vivo or in vitro, such as acetylation or carboxylation. The modifications also include glycosylation, such as proteins generated by conducting glycosylation during protein synthesis and processing or further processing steps. This modification can be achieved by exposure of the protein to an enzyme that glycosylates (such as mammalian glycosylase or deglycosylase). The modifications also include sequences with phosphorylated amino acid residues (e.g. phosphotyrosine, phosphoserine, phosphothreonine), and further include protein modified to improve its anti-proteolytic properties, or to optimize the solubility.

The term “nucleic acid” used herein be in the form of DNA or RNA. Forms of DNA includes cDNA, genomic DNA or artificially synthesized DNA. The DNA may be single-stranded or double-stranded. The DNA may be coding strand or non-coding strand. The coding sequence that encodes the mature protein can be identical with the sequence shown in the coding region of SEQ ID NO: 9, 10, 11, 12 or 13, or its degenerate variants. “Degenerate variant” used in the invention refers to a nucleic acid sequence that encodes the fluorescent fusion protein of the invention, but is different from the coding region sequence shown in SEQ ID NO: 9, 10, 11, 12 or 13.

In the context of nucleic acid, the term “variants” used herein may be naturally occurring allelic variants or non-naturally occurring variants. These nucleotide variants include degenerate variants, substituted variants, deletion variants, and insertion variants. As known in the art, allelic variant is an alternate form of a nucleic acid, it may be caused by one or more nucleotide substitution, deletion or insertion, but does not substantially alter the function of the encoded protein. The nucleic acid of the invention may include nucleotide sequences with at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 98%, at least about 99%, or 100% identity with said nucleic acid sequence.

As used herein, the term “hybridizing under stringent conditions” is used to describe conditions for hybridization and washing under which nucleotide sequences at least 60% homologous to each other typically remain hybridized to each other. Preferrably, stringent conditions are the conditions that under which sequences at least 65%, more preferably at least 70%, and even more preferably at least 80% or higher homologous to each other typically remain hybridized to each other. The stringent condition is known to a person of ordinary skills in the art. In one preferred, non-limiting example, the stringent conditions are: (1) hybridization and elution under relatively low ionic strength and relatively high temperature, such as 0.2×SSC, 1% SDS, 0° C.; or (2) hybridization at the addition of denaturing agent, 50% (v/v) methyl amide, 0.1% fetal calf serum/0.1% Ficoll, 42° C., etc; or (3) hybridization occurred only between two sequences at least 90%, more preferably no less than 95% homologous to each other. Furthermore, the protein encoded by the nucleic acid sequences capable of hybridization has the same biological function and activity as the mature protein shown in SEQ ID NO: 4, 5, 6, 7 or 8.

The present invention also relates to a nucleic acid fragment hybridizes with the sequence described above. As used here, the length of “nucleic acid fragment” contains at least 15 nucleotides, preferably at least 30 nucleotides, more preferably at least 50 nucleotides, and most preferably at least 100 or more nucleotides. The nucleic acid fragment can be used for nucleic acid amplification techniques (e.g. PCR).

Generally, the full-length sequences or the fragments of the fluorescent sensor or fusion protein in the invention can be obtained by PCR amplification method, recombination method or artificially synthetic method. For PCR amplification, primers can be designed according to the relevant nucleotide sequence disclosed by the invention, and in particular, the sequence of the open reading frame, and commercially available cDNA library, or cDNA library prepared by person skilled in the art using routine methods could be used as template, thereby, obtaining the corresponding sequences by amplification. For longer sequences, two or more individual PCR amplifications are typically desired, which are followed by ligating the separately amplified fragment together in a proper order.

Once the corresponding sequence is obtained, a large quantities of the sequences can be achieved by recombination. Typically, the sequences is cloned into a vector, which is subsequently transferred into cell, and then the corresponding polypeptide or protein can be obtained from the proliferated host cells by routine isolation and purification methods.

Furthermore, artificial synthesis can also be used to synthesize the corresponding sequence, especially when the fragment is short. Typically, multiple smaller fragments are synthesized first, and later linked together to produce a fragment with much longer sequence.

So far, the DNA sequence that encoding the protein herein (or its fragment, derivative, analog or variant) can be obtained solely by chemical synthesis. Said DNA sequence can be introduced subsequently into various available DNA molecules (e.g. vectors) and cells that are already known in the art. Through mutant PCR or chemical synthesis methods, a mutation can be introduced into the sequence of the protein of the invention.

As used herein, the terms “expression vector” and “recombinant vector” may be used interchangeably, and refer to a prokaryotic or eukaryotic expression vector known in the art, such as a bacterial plasmid, bacteriophage, yeast plasmid, plant cell virus, mammalian cell virus such as adenovirus, retroviral or other vectors, which can replicate and stabilize in the host organism. One important feature of these recombinant vectors is that they typically comprise expression control sequences. As used herein, the term “expression control sequence” refers to an element that regulates transcription, translation and expression of a target gene, and may be operably linked with the target gene, said element may be an origin of replication, a promoter, a marker gene or translation control elements, including enhancers, operons, terminators, ribosome binding sites, etc., and the selection of expression control sequence depends on the host cell used. In present invention, suitable recombinant vector includes, but not limited to, bacterial plasmid. In the context of recombinant expression vector, “operably linked” means the target nucleotide sequence and the regulatory sequence are linked in a way that allows expression of the nucleotide sequence. Suitable methods for constructing expression vector which comprises the coding sequence of the fusion protein and appropriate transcriptional/translational control signals are well known to the person skilled in the art. These methods include in vitro recombinant DNA techniques, DNA synthesis techniques, in vivo recombination techniques, etc. Said DNA sequence may be effectively linked to a proper promoter in the expression vector to direct mRNA synthesis. Representative examples of promoters include E. coli lac or trp promoter; λ phage PL promoter; eukaryotic promoters include CMV immediate early promoter, HSV thymidine kinase promoter, early and late SV40 promoter, retrovirus LTR, and some other promoters known to control expression of genes in prokaryotic or eukaryotic cells or their viruses. Expression vector further comprises a ribosome binding site for the initiation of translation, and a transcription terminator.

A person of ordinary skills in the art will understand that design of the recombinant expression vector can vary depending on the host cell to be transformed, desired expression level of the protein and other factors. In addition, the recombinant expression vector preferably contains one or more selective marker genes to provide phenotypic traits, such as dihydrofolate reductase, neomycin resistance in eukaryotic cells, or tetracycline or ampicillin resistance in E. coli, for the selection of transformed host cells.

In one embodiment, the coding sequence of the fluorescent sensor or fusion protein in present invention is double digested with BamHI and HindIII and ligated into the pRSET_(b) vector digested with BamHI and HindIII to obtain an E. coli recombinant expression vector. The expression vector of the present invention can be transferred into a host cell to produce a protein or peptide comprising the fusion protein. This transfer process may be carried out using routine transformation or transfection techniques well known to a person skilled in the art.

As used herein, the term “host cell”, also known as recipient cells, refers to cells capable of receiving and accommodating recombinant DNA molecule(s), which is the place for recombinant gene amplification. An ideal recipient cell should satisfy two criteria: easily available and proliferating. The “host cell” in present invention may include prokaryotic cells and eukaryotic cells, specifically, include bacterial cells, yeast cells, insect cells and mammalian cells.

The expression vector in present invention can be used to express the fluorescent sensor or fusion proteins in prokaryotic or eukaryotic cells. Accordingly, the present invention relates to a host cell, preferably E. coli, having the expression vector of the invention incorporated therein. The host cell can be any prokaryotic or eukaryotic cell, representative examples include: bacterial cells including E. coli, Streptomyces, Salmonella typhimurium, fungal cells such as yeast, plant cells, insect cells as Drosophila S2 or Sf9, animal cells as CHO, COS, 293 cells or Bowes melanoma cells, etc., host cells described above are inclusive but not limiting. Said host cells are preferably those advantageous for expression of the gene product or the fermentative production, such cells are well known and routinely used in the art, for example, various E. coli cells and yeast cells. In one embodiment of the present invention, E. coli BL21 is selected to construct a host cell that expresses the fusion protein of present invention. The choice of appropriate carrier, promoter, enhancer and host cells is evident to a person of ordinary skills in the art.

As used herein, the term “transformation” and “transfection”, “incorporating” and “transduction” refer to various techniques, already known in the art, to introduce exogenous nucleic acid (e.g., linear DNA or RNA (e.g., linearized vector or individual gene construct without vector)) or nucleic acid in the form of carrier (e.g., plasmids, cosmids, phage, phagemid, plasmid, transposon or other DNA) into a host cell, including calcium phosphate or calcium chloride coprecipitation, DEAE-mannan-mediated transfection, lipid transfection, natural competent cells, chemical-mediated transfer, or electroporation. When the host is a prokaryote such as E. coli, competent cells capable of absorbing DNA can be harvested after exponential growth phase, and treated with CaCl₂ method, the steps used therein are well known in the art. Another method uses MgCl₂. If necessary, the transformation can also be conducted by electroporation. When the host cell is a eukaryotic cell, DNA transfection methods can be used are as follows: calcium phosphate co-precipitation method, conventional mechanical methods such as microinjection, electroporation, liposome packaging, etc.

Transformed cell obtained thereby may be cultured using routine methods which are suitable for the expression in the host cells in order to express the fusion protein of the present invention. Depending on the host cells, the medium used for culture can be various conventional media. The culture is performed under conditions suitable for the growth of the host cells. When the host cells have grown to an appropriate cell density, the selected promoter is induced by an appropriate method (such as temperature shift or chemical induction), and the cells are further incubated for another period of time.

In the above method, the recombinant protein can be expressed within the cell, or on the cell membrane or secreted into extracellular environment. If desired, the recombinant protein can be isolated or purified using various separation methods based on its physical, chemical and other characteristics. These methods are well known to a person skilled in the art. Examples of such methods include, but not limited to: conventional refolding treatment, treatment with a protein precipitating agent (salting out), centrifugation, osmotic lysis of bacteria, ultra treatment, ultra centrifugation, molecular sieve chromatography (gel filtration), adsorption chromatography, ion exchange chromatography, high performance liquid chromatography (HPLC) and various other liquid chromatography techniques, and combinations thereof.

In one embodiment, the fluorescence sensor or a fusion protein of present invention is produced by fermentation of E. coli comprising the coding sequence of the fusion protein, followed by ammonium sulfate sedimentation, ion exchange chromatography, and purification using gel filtration chromatography to obtain the fluorescent sensor or a fusion protein of the invention in a pure form.

Uses of the fluorescent sensor or fusion protein of the present invention include, but not limited to, detection of NADH, detection of NADH in physiological state, detection of NADH in subcellular level, in situ detection of NADH, screening of drugs, diagnostics of diseases associated with NADH level.

Concentrations, contents, percentages, and other numerical values may be presented herein in a range format. It is to be understood that such range format is used merely for convenience and brevity, and it should be interpreted flexibly to include not only the numerical values explicitly recited as the upper and lower limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within said range as if each numerical values or sub range is explicitly recited.

EXAMPLES

The invention is further illustrated by the specific examples described below. It should be understood that these examples are merely illustrative, and do not limit the scope of the present invention.

Unless otherwise indicated, experimental protocols in the following examples generally adopt customary conditions, such as those described in Sambrook et al., Molecular Cloning: A Laboratory Guide “(New York, USA: Cold Spring Harbor Laboratory Press, 1989); or the conditions according to the manufacturer's recommendations. Unless otherwise indicated herein, all percentages and parts are by weight.

I. Experimental Materials and Reagents

Reagents: Unless otherwise indicated, all reagents were purchased from Shanghai Sinopharm Chemical Reagent Co. Ltd. (Shanghai, China).

Tag enzymes, buffer, dNTP for PCR amplification; protease, buffer, T4 DNA ligase, T4 DNA ligase buffer, T4 polynucleotide kinase (PNK), T4 PNK buffer used in molecular biological experiments were all from Fermentas (Vilnius, Lithuania).

Example 1 Construction and Expression of pRSET_(b)-ydiH-YFP-ydiH (D2)

1. Amplification of Nucleic Acid Sequence of cpYFP

The coding sequence of yellow fluorescent protein (cpYFP) was amplified using pMD19-cpYFP (Nagai, T. et al., Proc Natl Acad Sci U.S.A. 2001, V.98(6), pp. 3197-3202) (obtained from Protein Chemistry Laboratory, East China University of Science and Technology (Shanghai, China)) as the template, and cpYFP F and cpYFP R as primers, where the primer sequences (primers were synthesized by Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) are as follows:

P1: SpeI (SEQ ID NO: 23) GAAATCGAA ACTAGT TACAACAGCCACAACGTCTATATC P2: KpnI (SEQ ID NO: 24) CCAAGCTTCGG GGTACC GTTGTACTCCAGCTTGTG

PCR Reaction System

PCR system Template 1 μl Forward primer 0.5 μl Reverse primer 0.5 μl 10× Taq buffer 5 μl Taq enzyme 1 μl dNTP (10 mM) 1 μl ddH₂O 41 μl total 50 μl

PCR Reaction Conditions:

95° C.  5 min 95° C. 40 s 30 cycles {open oversize brace} 55° C. 40 s 72° C.  1 min 72° C. 10 min

PCR amplification product was electrophoresed on a 1% agarose gel for 30 minutes to obtain cpYFP fragments of about 750 bp. cpYFP fragments were recovered and purified from the gel using Sangon DNA fragment recovery kit (Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) according to the manufacturer's instructions.

2. Extraction of Desired Gene Sequence from Bacillus subtilis 168 Cells

a. Sample Processing

(i) Bacillus subtilis 168 was obtained from China General Microbiological Culture Collection Center (Cat. No. 1.1656).

(ii) According to the conditions as described, 100 μl cultured Bacillus subtilis 168 was taken to measure the optical density of the broth at 600 nm, where OD₆₀₀=0.1 refers to a density of 1×10⁷˜5×10⁷ cells/ml, the actual number of cells was calculated thereby. Then 1 ml TRIzol reagent (Invitrogen, California, USA) would be added per 1×10⁷ cells for processing.

(iii) A proper amount of broth was taken, centrifuged at 4° C., 5000 rpm for 10 minutes, and the supernatant was discarded.

(iv) Bacterial pellet was washed with 100 μl 1×TE buffer (10 mM Tris-HCl, 1 mM EDTA pH8.0, reagents were from Amresco corporation (Amresco, Ohio, USA)), and centrifuged at 5000 rpm for 10 minutes, and the supernatant was discarded.

(v) The bacterial pellet was resuspend in 100 μl 1×TE buffer (comprising 2 mg/ml lysozyme (from Majorbio Biotech Co. Ltd., Shanghai, China)) and incubated at 37° C. for 30 minutes.

b. Phase Separation

(i) One milliliter of TRIzol reagent (Invitrogen) was added thereto and mixed by pipetting, and the mixture was allowed to stand at room temperature for 5 minutes.

(ii) Two hundred microliter of chloroform was added thereto and vortexed for 15 seconds, and the mixture was allowed to stand at room temperature for 2 to 3 minutes prior to centrifugation at 4° C., 12,000 g for 15 minutes.

(iii) The solution was segmented into layers upon centrifugation, comprising about 40% of upper aqueous phase containing RNA, and about 60% of lower organic phase containing DNA and protein. The upper aqueous phase was carefully pipetted out and removed.

c. Removal of Impurities

Fifty microliter of 10% SDS and 250 μl saturated aqueous sodium chloride solution were added into the organic phase, and vortexed to homogenous prior to centrifugation at 4° C., 12,000 g for 5 minutes, and the upper aqueous phase was discarded.

d. Ethanol Precipitation of DNA

Seven hundred and fifty microliter of precooled 95% ethanol was added into the organic phase and inverted to mix, and stand at −80° C. for 15 minutes to allow the DNA to precipitate.

e. DNA Washing

(i) The upper organic phase was carefully discarded.

(ii) The precipitate was washed several times with 1 ml of 0.1 M sodium citrate/10% ethanol solution, centrifugation at 4° C., 12,000 g for 5 minutes was conducted after each wash.

(iii) A final wash was conducted with 75% ethanol and followed by centrifugation at 4° C., 12000 g for 5 minutes.

(iv) The ethanol was evaporated through air dry at room temperature.

f. Dissolving DNA

DNA pellet was dissolved into 50 μl of 8 mM NaOH solution, and stored at 4° C. or −20° C.

The gene for YdiH protein of Bacillus subtilis 168 (ydiH), in full length or fragment thereof (for amino acids 85-215), was amplified using genomic material extracted above as the template, and primers ydiH-1F and ydiH 1R, ydiH(D2) 2F and ydiH 2R, respectively, wherein amplification with ydiH-1F and ydiH 1R produced ydiH1, the full length YdiH protein gene (ydiH) having BaHI restriction site at 5′ end and SpeI restriction site at 3′ end; amplification with ydiH (D2) 2F and ydiH 2R produced ydiH(D2) 2, a fragment of YdiH Protein gene (ydiH) (for amino acids 85-215) having KpnI restriction site at 5′ end and HindIII restriction site at 3′ end. Sequences of the primers ydiH 1F, ydiH 1R, ydiH (D2) 2F and ydiH 2R are as follows:

ydiH 1F: BamHI (SEQ ID NO: 25) CC GGATCC ATGAATAAGGATCAATCAAAAATTC ydiH 1R: SpeI (SEQ ID NO: 26) GCTGTTGTA ACTAGT TTCGATTTCCTCTAAAACT ydiH(D2) 2F: KpnI (SEQ ID NO: 27) CGG GGTACC ATGACAGACGTCATCTTGATTGGTG ydiH 2R: HindIII (SEQ ID NO: 28) CCC AAGCTT CTATTCGATTTCCTCTAAAAC

PCR Reaction System:

PCR system Template 1 μl Forward primer 0.5 μl Reverse primer 0.5 μl 10× Taq buffer 5 μl Taq enzyme 1 μl dNTP (10 mM) 1 μl ddH₂O 41 μl total 50 μl

PCR Reaction Conditions:

95° C.  5 min 95° C. 40 s 30 cycles {open oversize brace} 55° C. 40 s 72° C.  1 min 72° C. 10 min

PCR amplification product was purified on 1% agarose gel by electrophoresis for 30 minutes to obtain the ydiH 1 of about 700 bp and ydiH (D2) 2 fragment of about 450 bp. The amplified ydiH 1 and ydiH (D2) 2 fragments were recovered and purified from the gel using Sangon DNA fragment recovery and purification kit (Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) according to the manufacturer's instructions.

3. Ligation of the Target Gene Fragment to the Vector

Overlap extension PCR was conducted using ydiH 1 and cpYFP as templates, and ydiH 1F and cpYFP 1R as primers with the following PCR system:

PCR system Template 1⁽¹⁾ 1 μl Template 2⁽¹⁾ 1 μl Forward primer⁽²⁾ 0.5 μl Reverse primer⁽²⁾ 0.5 μl 10× pfu buffer 5 μl pfu enzyme 1 μl dNTP (10 mM) 1 μl ddH₂O 40 μl total 50 μl ⁽¹⁾Template fragments need to be purified. ⁽²⁾The forward and reverse primers were initially absent in the reaction system but added after 10 cycles.

PCR Reaction Conditions:

PCR reaction conditions 95° C.  5 min 95° C. 40 s 10 cycles {open oversize brace} 55° C. 40 s 72° C. 1 min 15 s 95° C. 40 s 20 cycles {open oversize brace} 58° C. 40 s 72° C. 2 min 10 s 72° C. 10 min

PCR amplification product was subjected to electrophoresis on 1% agarose gel for 40 minutes for the ydiH-cpYFP fragment of about 1400 bp. The recovered and purified PCR fragment ydiH-YFP and vector plasmid pRSET_(b) were double digested separately with the following digestion systems:

Double enzyme digestion system Vector plasmid pRSET_(b) 10 μl BamHI  1 μl HindIII  2 μl 10x BamHI buffer  5 μl ddH₂O 32 μl total 50 μl

Double enzyme digestion system DNA fragment ydiH-YFP 15 μl BamHI  1 μl HindIII  2 μl 10x BamHI buffer  5 μl ddH₂O 27 μl Total 50 μl

Reaction conditions: 37° C., 5 hours.

After the reaction was concluded, 10 μl of 6× loading buffer was added to the 50 μl reaction system to stop the reaction. Then target fragments were isolated by agarose gel electrophoresis, recovered and purified using Sangon DNA fragment recovery kit (Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) according to the manufacturer's instructions.

The double digested fragment of ydiH-cpYFP and the double digested fragment of vector plasmid pRSET_(b) recovered above were ligated using the following systems:

Ligation system DNA fragment ydiH-YFP 4 Fragment pRSET_(b) vector 1 T4 DNA ligase 0.5 10x T4 DNA ligase buffer 1 ddH₂O 3.5 total 10

Reaction conditions: 16° C., overnight. Ligated product pRSET_(b)-ydiH-YFP was formed thereby.

Finally, ydiH (D2) 2 described above and validated pRSET_(b)-ydiH-YFP were double digested as following:

Double enzyme digestion system DNA fragment ydiH(D2) 2 15 μl KpnI  1 μl HindIII  3 μl 10x KpnI buffer  5 μl ddH₂O 26 μl Total 50 μl

Double enzyme digestion system Vector plasmid 10 μl pRSET_(b)-ydiH-YFP KpnI  1 μl HindIII  2 μl 10x KpnI buffer  5 μl ddH₂O 32 μl total 50 μl

Reaction conditions: 37° C. for 5 hours.

When the reaction was concluded, 10 μl of 6× loading buffer was added to the 50 μl reaction system to terminate the reaction. Target fragments were then isolated by agarose gel electrophoresis, recovered and purified using Sangon DNA fragment recovery kit (Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) according to the manufacturer's instructions.

As described above, the double digested product of ydiH (D2) 2 and pRSET_(b)-ydiH-YFP were recovered and ligated to form the final ligation product pRSET_(b)-ydiH-YFP-ydiH(D2).

Positive colonies identified by PCR identification were selected, and sequenced using universal primers at the Shanghai Branch of Beijing Liuhe BGI Technology Co., Ltd. The sequence data was analysed and compared using Vector NTI 8.0. The results showed that the plasmid was actually comprising inserted nucleotide sequence of ydiH-cpYFP-ydiH (D2) (sequence shown as SEQ ID NO: 9 in the sequence listing), which encodes the protein shown as SEQ ID NO: 4 in the sequence listing.

4. Transformation

The recombinant plasmid pRSET_(b)-ydiH-cpYFP-ydiH (D2) was transformed into competent E. coli BL21 (DE3) pLysS (purchased from Tiangen Biotech Co. Ltd., Beijing, China) to obtain recombinant E. coli BL-Frex, the detailed process is as follows:

(i) One microliter of plasmid or 10 μl of ligation product was added to 100 μl competent bacteria under sterile condition, then kept in ice bath for 45 minutes;

(ii) After ice bathing, the mixture was immediately heat shocked in a 42° C. water bath for 90 to 120 seconds;

(iii) Subjected to ice bath for another 5 minutes;

(iv) Recovered by adding 800 μl LB liquid medium and incubating at, 150 rpm on a shaker for 1 hour;

(v) Centrifuged at 4000 rpm for 5 minutes at room temperature, the supernatant was discarded;

(vi) The pellet was resuspended into a small amount of fresh LB, the entire suspension was then evenly spreaded on LB plates, which were inverted and incubated overnight at 37° C.

Positive colonies were selected using conventional Colony PCR, transferred to 5 ml LB liquid medium containing the appropriate selective pressure, and cultured overnight at 37° C., 220 rpm. The recombinant strain BL-Perex was cultured in LB medium at 37° C., and 0.1 mM IPTG was added when the OD for cell concentration reached 0.8. The expression was induced at 18° C. for 20 hours, and F-rex1 protein was isolated and purified from the bacterial lysate using Ni²⁺ affinity chromatography column (General Electric Company, Uppsala, Sweden). The SDS-PAGE identified only one protein band at approximately 66.5 kD, which was the F-rex1 protein (FIG. 1). As shown in FIG. 1, band 1 is the F-rex protein purified by Ni²⁺ affinity chromatography column, and band 2 is the marker.

Example 2 Construction and Expression of pRSET_(b)-ydiH(189)-YFP-ydiH(190)

1. Amplification the Nucleic Acid Sequence of cpYFP:

The coding sequence of yellow fluorescent protein (cpYFP) was amplified using pMD19-cpYFP as the template, and cpYFP F and cpYFP R as primers, where the primer sequences (primers were synthesized by Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) are as follows:

P1: PstI (SEQ ID NO: 29) GAAT CTGCAG GCTACAACAGCCACAACGTCTATATC P2: KpnI (SEQ ID NO: 30) CCAAGCTTCGG GGTACC GTTGTACTCCAGCTTGTG

PCR Reaction System

PCR system Template 1 μl Forward primer 0.5 μl   Reverse primer 0.5 μl   10x Pfu buffer 5 μl Pfu enzyme 1 μl dNTP (10 mM) 1 μl ddH₂O 41 μl  total 50 μl 

PCR Reaction Conditions:

95° C.  5 min 95° C. 30 s 30 cycles {open oversize brace} 55° C. 30 s 72° C. 1 min 15 s 72° C. 10 min

PCR amplification product was electrophoresed on 1% agarose gel for 20 minutes to obtain cpYFP fragment of approximately 750 bp. cpYFP fragments were recovered and purified from the gel using Sangon DNA fragment recovery kit (Sangon Biotech (Shanghai) Co., Ltd., Shanghai, China) according to the manufacturer's instructions.

2. Amplification of Target Gene Sequence for YdiH Protein of Thermus aquaticus

The gene T-ydiH for YdiH protein of Thermus aquaticus was synthesized by Shanghai Generay Biotech Co. Ltd. (Shanghai, China) (synthesized according to the full-length gene sequence deposited in NCBI GenBank, NCBI Genbank AF061257.1).

Then the full length T-ydiH sequence for YdiH protein of Thermus aquaticus was amplified using the gene described above as the template, and ydiH IF and ydiH 2R as primers. The amplification using primers ydiH IF and ydiH 2R produced YdiH in full length for T-YdiH protein and having BamHI digestion site at 5′ end and HindIII digestion site at 3′ end, wherein the sequences of primer ydiH F and ydiH of 2R are as follows:

P3: BamHI (SEQ ID NO: 31) CC GGATCC GATGAATAAGGATCAATCAAAAATTC P4: HindIII (SEQ ID NO: 32) CCC AAGCTT CTATTCGATTTCCTCTAAAAC

PCR Reaction System

PCR system Template 1 μl Forward Primer 0.5 μl   Reverse Primer 0.5 μl   10x Pfu buffer 5 μl Pfu enzyme 1 μl dNTP (10 mM) 1 μl ddH₂O 41 μl  total 50 μl 

PCR Reaction Conditions:

95° C.  5 min 95° C. 40 s 30 cycles {open oversize brace} 55° C. 40 s 72° C.  1 min 72° C. 10 min

PCR amplification products was purified on 1% agarose gel by electrophoresis for 30 minutes to obtain the T-ydiH1 fragment of about 700 bp. The amplified T-ydiH fragment was recovered and purified using Sangon DNA fragment recovery purification kit (Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) according to the manufacturer's instructions.

3. Ligation of the Target Gene to the Vector

The recovered and purified PCR fragment T-ydiH and vector plasmid pRSET_(b) were double digested separately with the following system:

Double enzyme digestion system DNA fragment T-ydiH 15 μl BamHI  1 μl HindIII  2 μl 10x BamHI buffer  5 μl ddH₂O 27 μl total 50 μl

Double enzyme digestion system Vector plasmid pRSET_(b) 10 μl BamHI  1 μl HindIII  2 μl 10x BamHI buffer  5 μl ddH₂O 32 μl Total 50 μl

Reaction conditions: 37° C. for 5 hours.

After the reaction was concluded, 10 μl of 6× loading buffer was added to the 50 μl reaction system to stop the reaction. Then target fragments were isolated by agarose gel electrophoresis, recovered and purified using Sangon DNA fragment recovery kit (Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) according to the manufacturer's instructions.

The double digested fragment of T-ydiH and the double digested fragment of vector plasmid pRSET_(b) as recovered above were ligated using the following system:

Ligation system DNA fragment T-ydiH-YFP 4 Fragment pRSET_(b) vector 1 T4 DNA ligase 0.5 10x T4 DNA ligase buffer 1 ddH₂O 3.5 total 10

Reaction conditions: 16° C. overnight. Ligated product pRSET_(b)-ydiH was formed thereby.

The full length pRSET_(b)-ydiH sequence was amplified using the validated PRSET_(b)-ydiH as a template, T-ydiH(L190) F and T-ydiH (F189) R as primers. The amplification using primers T-ydiH(L190) F and T-ydiH (F189) R produced a full length fragment ydiH-pRSET_(b) of the pRSET_(b)-ydiH having PstI digestion site at 5′ end and KpnI digestion site at 3′ end, wherein the sequences of primers T-ydiH (L190) F and T-ydiH (F189) R are as follows:

P5: KpnI (SEQ ID NO: 33) ATA GGTACC GGCCTGGCCGGCCTGACCCGGCTG P6: PstI (SEQ ID NO: 34) ATA CTGCAG AGAAGTCCACGTTCTCCACGGCCACCTC

Finally, the yidH-pRSET_(b) fragment produced thereby, and validated cpYFP fragment were double digested under following conditions:

Double enzyme digestion system DNA fragment cpYFP 15 μl KpnI 1.5 μl  PstI 1.5 μl  10x BamHI buffer  5 μl ddH₂O 27 μl total 50 μl

Double enzyme digestion system DNA fragment yidH-pRSET_(b) 10 μl KpnI 1.5 μl  PstI 1.5 μl  10x BamHI buffer  5 μl ddH₂O 32 μl total 50 μl

Reaction conditions: 37° C., 5 hours.

After the reaction was concluded, 10 μl of 6× loading buffer was added to the 50 μl reaction system to terminate the reaction. Then target fragments were isolated by agarose gel electrophoresis, recovered and purified using Sangon DNA fragment recovery kits (Sangon Biotech (Shanghai) Co. Ltd., Shanghai, China) according to the manufacturer's instructions.

The double digested fragments of yidH-pRSET_(b) and cpYFP as recovered above were ligated to form the final product pRSET_(b)-ydiH (189)-YFP-ydiH (190).

Positive colonies identified by Colony PCR were selected, sequenced using universal primers at the Shanghai Brance of Beijing Liuhe BGI Technology Co. Ltd. The determined sequence was compared and analysed using Vector NTI 8.0. The result showed that this plasmid was actually comprising inserted nucleotide sequence of ydiH (189)-YFP-ydiH (190) (sequence shown as SEQ ID NO: 13), and which encodes the protein shown as SEQ ID NO: 8 in the sequence listing.

4. Transformation

Recombinant plasmid pRSET_(b)-ydiH(189)-YFP-ydiH(190) was transformed into competent E. coli BL21 (DE3) pLysS (purchased from TIANGEN Biotech Co. Ltd., Beijing, China) to obtain the recombinant strain BL-Frex, the detailed process is as follows:

(i) One microliter of plasmid or 10 μl of ligation product was added to 100 μl of competent bacteria under sterile condition, then kept in ice bath for 45 minutes;

(ii) After ice bathing, the mixture was immediately heat shocked in a 42° C. water bath for 90 to 120 seconds;

(iii) Subjected to ice bath for another 5 minutes;

(iv) Recovered by adding 800 μl LB liquid medium, and incubating at 37° C., 220 rpm on a shaker for 1 hour;

(v) Centrifuged at 4000 rpm for 5 minutes at room temperature, and the supernatant was discarded;

(vi) The pellet was resuspended into a small amount of fresh LB, and the entire suspension was then evenly spreaded on LB plates, which were inverted and incubated overnight at 37° C.

Positive colonies were selected using conventional Colony PCR, transferred to 5 ml LB liquid medium containing the appropriate selective pressure, and cultured overnight at 37° C., 220 rpm. The recombinant strain BL-Perex was cultured at 37° C., and 0.1 mM IPTG was added when the OD of cell concentration reached 0.8. The expression was induced at 18° C. for 20 hours, and F-rex2 protein was isolated and purified from the bacterial lysate using Ni²⁺ affinity chromatography column (General Electric Company, Uppsala, Sweden). The SDS-PAGE identified only one protein band at approximately 50 kD, which was the F-rex2 protein (FIG. 2). As shown in FIG. 12, band 1 is the F-rex2 protein purified by Ni²⁺ affinity chromatography column, while band 2 is the marker.

Example 3 Derivatives of YdiH-YFP-ydiH (D2) Sensors

Principle for Sensor Construction

Derivative sensors were engineered using intermediate plasmids for the construction of pRSET_(b)-ydiH-YFP-ydiH and other sensors as templates, and following the principle of site-directed mutagenesis.

Truncated mutant sequences are shown below:

SEQ Original sequence 206 KHYSVLEEIE 215-TS-YFP-GT-ydiH ID NO Del T(2) 206 KHYSVLEEIE 215-TS-YFP-G-ydiH 104 Del G 206 KHYSVLEEIE 215-TS-YFP-T-ydiH 103 Del GT 206 KHYSVLEEIE 215-TS-YFP-ydiH 102 Del S 206 KHYSVLEEIE 215-T-YFP-GT-ydiH 126 Del T(1) 206 KHYSVLEEIE 215-S-YFP-GT-ydiH 101 Del TS 206 KHYSVLEEIE 215-YFP-GT-ydiH 159 C9 206 KHYSVLEEI 214-YFP-GT-ydiH 100 C8 206 KHYSVLEE 213-YFP-GT-ydiH 99 C2 206 KH 207-YFP-GT-ydiH 93 C1 206 K-YFP-GT-ydiH 92

Establishment of the Mutant Library

1. Primer Design (Shanghai Sangon)

SEQ ID No Remark Sequence(5′-3′) 35 C9 Reverse GATTTCCTCTAAAACTGAATAATGCTTC 36 C8 Reverse TTCCTCTAAAACTGAATAATGCTTC 37 C6 Reverse TAAAACTGAATAATGCTTCAAAAAATAA ACCAG 38 C5 Reverse AACTGAATAATGCTTCAAAAAATAAACCAG 39 C4 Reverse TGAATAATGCTTCAAAAAATAAACCAG 40 C3 Reverse ATAATGCTTCAAAAAATAAACCAGTG 41 C2 Reverse ATGCTTCAAAAAATAAACCAGTGACTG 42 C1 Reverse CTTCAAAAAATAAACCAGTGACTGAAGC 43 C9 Forward TACAACAGCGACAACGTC (general forward primer for C series) 44 C7 Reverse CTCTAAAACTGAATAATGCTTC 45 Del GT Forward ATGACAGACGTCATCTTGATTG 46 Del GT Reverse GTTGTACTCCAGCTTGTGCC 47 Del TS Forward TACAACAGCGACAACGTCTATATCATG 48 Del TS Reverse TTCGATTTCCTCTAAAACTGAATAATGC 49 Del T(1) AGTTACAACAGCGACAACGTCTATATCATG Forward 50 Del S-deletion AGTTTCGATTTCCTCTAAAACTGAATAATGC Reverse 51 Del G-deletion ACCATGACAGACGTCATCTTGATTG Forward 52 Del T(2)- ACCGTTGTACTCCAGCTTGTGCC deletion Reverse 53 D118K Forward TTTTAAGATAAATGAGAGTAAAATAGG 54 118/120 GCCATAGAAATTTTTGTGTTATTG mutation Reverse 55 D118R Forward TTTTCGGATAAATGAGAGTAAAATAGG 56 N120K Forward TTTTGATATAAAGGAGAGTAAAATAGG 57 N120R Forward TTTTGATATACGGGAGAGTAAAATAGG 58 N120E Forward TTTTGATATAGAAGAGAGTAAAATAGG 59 N120D Forward TTTTGATATAGATGAGAGTAAAATAGG 60 D193N Forward TAAATTTAGCAGTTGAGCTTCAG 61 193/194 TATGATGAATTCGAATGTGTTC mutation Reverse 62 D193K Forward TAAAGTTAGCAGTTGAGCTTCAG 63 D193R Forward TACGGTTAGCAGTTGAGCTTCAG 64 L194E Forward TAGATGAAGCAGTTGAGCTTCAG 65 L194D Forward TAGATGATGCAGTTGAGCTTCAG 66 L194K Forward TAGATAAGGCAGTTGAGCTTCAG 67 L194R Forward TAGATCGGGCAGTTGAGCTTCAG

2. PCR Amplification

Truncated mutation and site-directed mutation were conducted using site-directed mutagenesis PCR.

Amplification system for PCR mutation (primer, enzyme, dNTP and others purchased from Fermentas):

PCR sampling system Template 0.1 μl Forward Primer 0.5 μl Reverse Primer 0.5 μl 5x PrimeStar Buffer  10 μl PrimeStar polymerase 0.5 μl dNTP mix(10 mM)   4 μl ddH₂O 33.5 μl  Total  50 μl

PCR reaction conditions 98° C.   5 min 98° C.  10 sec 30 cycles {open oversize brace} 55° C.   5 sec 72° C. 4.5 min 72° C.  10 min

3. Separation, Purification of DNA Fragments

DpnI Digestion

The PCR amplified fragment was first treated with DpnI enzyme (from Fermentas) for 3 hours at 37° C. to remove the potential template plasmid contamination. The reaction system was then denatured and deactivated at 80° C. for 20 minutes. The deactivated mixture could be directly used for subsequent molecular biological experiments.

Phosphorylation of DNA Fragment

At the presence of ATP, the DNA fragment was treated with T4 polynucleotide kinase (T4 PNK) (from Fermentas) at 37° C. for 1 h to phosphorylate the 5′-OH of DNA ribose ring, in order to allow the fragments to cyclize by self-ligation. Then the reaction system was denatured and deactivated at 75° C. for 10 minutes. The deactivated mixture could be directly used for subsequent molecular biological experiments.

Ligation

The phosphorylated DNA fragments (mutated DNA fragments: pRSET_(b)-ydiH-YFP or pRSET_(b)-YFP-ydiH) were cyclized by self ligation overnight at 16° C. with T4 DNA ligase enzyme (from Fermentas).

Double-Digestion of Mutant Plasmids

The extracted mutant plasmids pRSET_(b)-ydiH-YFP series and pRSET_(b)-YFP-ydiH series were double digested, respectively. The digestion systems are as follows:

Double-digest system Mutant plasmid 10 μl pRSET_(b)-ydiH-YFP series BsrGI  1 μl HindIII  2 μl 10x Tango buffer  5 μl ddH₂O 32 μl Total 50 μl

Double-digest system Mutant plasmid 10 μl pRSET_(b)-YFP-ydiH series BsrGI  1 μl HindIII  2 μl 10x Tangobuffer  5 μl ddH₂O 32 μl Total 50 μl

Reaction conditions: 37° C. for 5 h.

When the reaction was concluded, 10 μl of the 6× loading buffer was added to the 50 μl reaction system to terminate the reaction. The fragment was isolated by agarose gel electrophoresis, recovered and purified using adsorption column Detailed steps are described in “Shanghai Sangon Gel Purification Kits/DNA Recovery Kits”.

For truncated mutations, digested fragment of pRSET_(b)-ydiH-YFP from proper mutant plasmid of pRSET_(b)-ydiH-YFP series was selected as desired, and then ligated with normal fragment of sequence YFP-ydiH without mutation. For site-directed mutagenesis, digested fragment of pRSET_(b)-ydiH-YFP from proper mutant plasmid of pRSET_(b)-ydiH-YFP series was selected as desired, and then ligated with digested fragment YFP-ydiH of pRSET_(b)-ydiH-YFP series containing site-directed mutation as well.

Ligation

Recovered and purified fragments pRSET_(b)-ydiH-YFP and YFP-ydiH were ligated using the following system:

Ligation system Fragment YFP-ydiH 4 Fragment pRSET_(b)-ydiH-YFP 1 T4 DNA Ligase enzyme 0.5 10x T4 DNA Ligase buffer 1 ddH₂O 3.5 Total 10

Reaction conditions: 16° C., overnight.

The ligation products were labeled to form pRSET_(b)-ydiH-YFP-ydiH Truc v2.xx or pRSET_(b)-ydiH-YFP-ydiH.

Identification of Plasmid Mutations

Colonies identified as positive in Colony PCR were selected and sequenced using universal primers at the Shanghai Branch of Beijing Liuhe BGI Technology Co., Ltd. The determined sequences were then compared and analyzed by Vector NTI 8.0.

Construction of Sensor Series

Following sensors were produced according to the methods described above.

Plasmid NO. SEQ ID NO pRSET_(b)-ydiH-YFP-ydiH(D2)C1 C1 92 pRSET_(b)-ydiH-YFP-ydiH(D2)C2 C2 93 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 C3 94 pRSET_(b)-ydiH-YFP-ydiH(D2)C4 C4 95 pRSET_(b)-ydiH-YFP-ydiH(D2)C5 C5 96 pRSET_(b)-ydiH-YFP-ydiH(D2)C6 C6 97 pRSET_(b)-ydiH-YFP-ydiH(D2)C7 C7 98 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 C8 99 pRSET_(b)-ydiH-YFP-ydiH(D2)C9 C9 100 pRSET_(b)-ydiH-YFP-ydiH(D2)Del T Del T(1) 101 pRSET_(b)-ydiH-YFP-ydiH(D2)Del GT Del GT 102 pRSET_(b)-ydiH-YFP-ydiH(D2)Del G Del G 103 pRSET_(b)-ydiH-YFP-ydiH(D2)Del T Del T(2) 104 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 D118R C3 D118R 105 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 N120K C3 N120K 106 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 N120R C3 N120R 107 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 N120E C3 N120E 108 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 N120D C3 N120D 109 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 D193N C3 D193N 110 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 D193K C3 D193K 111 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 L194K C3 L194K 112 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 L194R C3 L194R 113 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 L194E C3 L194E 114 pRSET_(b)-ydiH-YFP-ydiH(D2)C3 L194D C3 L194D 115 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 D118R C8 D118R 116 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 N120K C8 N120K 117 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 N120R C8 N120R 118 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 N120E C8 N120E 119 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 N120D C8 N120D 120 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 D193N C8 D193N 121 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 D193K C8 D193K 122 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 L194K C8 L194K 123 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 L194R C8 L194R 124 pRSET_(b)-ydiH-YFP-ydiH(D2)C8 L194E C8 L194E 125

Example 4 Derivative Sensors of ydiH(189)-YFP-ydiH(190)

Principle for Sensor Construction

Derivative sensors were engineered using intermediate plasmid for constructing sensors such as pRSET_(b)-ydiH(189)-YFP-ydiH(190) as templates and following the principle of site-directed mutagenesis.

Truncated mutant sequences are shown below:

Name Structure SEQ ID NO Original sequence F189-SAG-YFP-GGC-L190 127 189/190-N1 F189-AG-YFP-GGC-L190 128 189/190-N2 F189-G-YFP-GGC-L190 129 189/190-N3 F189-YFP-GGC-L190 130 189/190-C1 F189-SAG-YFP-GG-L190 131 189/190-C2 F189-SAG-YFP-G-L190 132 189/190-C3 F189-SAG-YFP-L190 133 189/190-C1N1 F189-AG-YFP-GG-L190 134 189/190-C1N2 F189-G-YFP-GG-L190 135 189/190-C1N3 F189-YFP-GG-L190 136 189/190-C2N1 F189-AG-YFP-G-L190 137 189/190-C2N2 F189-G-YFP-G-L190 138 189/190-C2N3 F189-YFP-G-L190 139 189/190-C3N1 F189-AG-YFP-L190 140 189/190-C3N2 F189-G-YFP-L190 141 189/190-C3N3 F189-YFP-L190 142

Establishment of Mutant Library

1. Primer Design (Shanghai Sangon)

SEQ ID No Remark Sequence(5′-3′) 68 189/190-N1 (F) GCAGGCTACAACAGCGACAACGTC 69 189/190-N1 (R) GAAGTCCACGTTCTCCACGGCCAC 70 189/190-N2 (F) GGCTACAACAGCGACAACGTCTATATCATG 71 189/190-N3 (F) TACAACAGCGACAACGTCTATATCATGGC 72 189/190-C1 (F) CTGGCCGGCCTGACCCGGCTGAG 73 189/190-C1 (R) GGTACCGTTGTACTCCAGCTTGTGCCCCAGG 74 189/190-C2 (R) ACCGTTGTACTCCAGCTTGTGCCCCAGGATG 75 189/190-C3 (R) GTTGTACTCCAGCTTGTGCCCCAGGATGTTG C 76 Trex(D2) (F) ATGAACCGGAAGTGGGGCCTG 77 Trex(D2) (R) CGGATCCTTATCGTCATCGTCGTAC 78 D112SV113H (F) CATGACCCCGAGAAGGTGGGC 79 D112SV113H (R) CGAGAAGAAGCCCCGCAGCTC

2. PCR Amplification

Truncated mutation and site-directed mutation were conducted using site-directed mutagenesis PCR.

Amplification system for PCR mutation (Primer, enzyme, dNTP and others purchased from Fermentas):

PCR reaction conditions 98° C.   5 min 98° C.  10 sec 30 cycles {open oversize brace} 55° C.   5 sec 72° C. 4.5 min 72° C.  10 min

PCR amplification system Template 0.1 μl Forward Primer 0.5 μl Reverse Primer 0.5 μl 5x PrimeStar Buffer  10 μl PrimeStar polymerase 0.5 μl dNTP mix(10 mM)   4 μl ddH₂O 33.5 μl  Total  50 μl

3. Separation, Purification of DNA Fragments

DpnI Digestion

The PCR amplified fragment was first treated with DpnI enzyme (from Fermentas) for 3 hours at 37° C. to remove the potential template plasmid contamination. The reaction system was then denatured and deactivated at 80° C. for 20 minutes. The deactivated mixture could be directly used for subsequent molecular biological experiments.

Phosphorylation of DNA Fragment

At the presence of ATP, the DNA fragment was treated with T4 polynucleotide kinase (T4 PNK) (from Fermentas) at 37° C. for 1 h to phosphorylate the 5′-OH of DNA ribose ring, in order to allow the fragment to cyclize by self-ligation. Then the reaction system was denatured and deactivated at 75° C. for 10 minutes. The deactivated mixture could be directly used for subsequent molecular biological experiments.

Ligation

The phosphorylated DNA fragments (mutated DNA fragments: pRSET_(b)-ydiH-YFP or pRSET_(b)-YFP-ydiH) were cyclized by self ligation overnight at 16° C. with T4 DNA ligase enzyme (from Fermentas).

Identification of Plasmid Mutations

Colonies identified as positive in Colony PCR were selected and sequenced using universal primers at the Shanghai Branch of Beijing Liuhe BGI Technology Co., Ltd. The determined sequence was then compared and analyzed by Vector NTI 8.0.

Construction of Sensor Series

Following sensors were produced according to the methods described above, and numbered respectively.

SEQ ID Plasmid NO. NO pRSET_(b)-ydiH(189)-YFP-ydiH(190) F-rex2-1.0 127 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-N1 F-rex2-2.0 128 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-N2 F-rex2-2.1 129 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-N3 F-rex2-2.2 130 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C1 F-rex2-2.3 131 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C2 F-rex2-2.4 132 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C3 F-rex2-2.5 133 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C1N1 F-rex2-2.6 134 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C1N2 F-rex2-2.7 135 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C1N3 F-rex2-2.8 136 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C2N1 F-rex2-2.9 137 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C2N2 F-rex2-2.10 138 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C2N3 F-rex2-2.11 139 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C3N1 F-rex2-2.12 140 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C3N2 F-rex2-2.13 141 pRSET_(b)-ydiH(189)-YFP-ydiH(190)-C3N3 F-rex2-2.14 142 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190) F-rex2-2.15 143 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-N1 F-rex2-2.16 144 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-N2 F-rex2-2.17 145 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-N3 F-rex2-2.18 146 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C1 F-rex2-2.19 147 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C2 F-rex2-2.20 148 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C3 F-rex2-2.21 149 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C1N1 F-rex2-2.22 150 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C1N2 F-rex2-2.23 151 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C1N3 F-rex2-2.24 152 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C2N1 F-rex2-2.25 153 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C2N2 F-rex2-2.26 154 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C2N3 F-rex2-2.27 155 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C3N1 F-rex2-2.28 156 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C3N2 F-rex2-2.29 157 pRSET_(b)-Trex(D2)-ydiH(189)-YFP-ydiH(190)-C3N3 F-rex2-2.30 158

Example 5 Spectral Characteristics of Fluorescent Sensors for NADH

The fluorescent sensors that prepared above were dissolved in assay buffer (100 mM KPi, pH7.4) to formulate fluorescent sensor solutions to a final concentration of 10 μM. Then their absorption spectra were measured using a Multi-functional Fluorescence Microplate Reader (Synergy2, Biotek) (FIG. 3A).

Their excitation and emission spectra were determined using a fluorescence spectrophotometer (Cary Eclipse Fluorescence spectrophotometer, Varian) (FIG. 3B).

Experimental results indicated that, F-rex1 had two excitation peaks at 400 nm and 490 nm, respectively, and the latter exhibited an intensity five times of that of the former. However, F-rex1 had only one emission peak at 521 nm. Meanwhile, F-rex2 protein has two excitation peaks at 410 nm and 500 nm, respectively, and the latter exhibited an intensity about half of that of the former. However, F-rex2 had only one emission peak at 518 nm (FIG. 4).

Example 6 Characteristics of Fluorescent Sensors for NADH in Responses to Pyridine Nucleotide Analogs Under Physiological Conditions

The fluorescent sensors prepared above were dissolved in assay buffer (100 mM KPi, pH7.4) to formulate protein solutions to a final concentration of 1 μM. Pyridine nucleotide analogs NAD⁺, NADH, ATP, ADP, NADP⁺ and NADPH (Merck Biosciences GmbH, Darmstadt, Germany) were prepared in assay buffer (100 mM KPi, pH7.4) for stock solutions at a final concentration of 8 mM, which were diluted to 80 μM before use.

Two hundred microliter of the 1 μM solution of fluorescent sensors was taken, and first titrated 5× with 4 μl of the 80 μM NAD⁺ or NADH or ATP or ADP or NADP⁺ or NADPH, then further titrated 5× with 4 μl of the 8 mM NAD⁺ or NADH or ATP or ADP or NADP⁺ or NADPH. After each titration, the solution was vortexed 5 seconds to allow the reaction to complete, then the fluorescent intensity of 528 nm emission upon 485 nm excitation was measured using a Multi-functional Fluorescence Microplate Reader (Synergy2, Biotek).

Measurements demonstrated that, NADH fluorescent sensors exhibited robust response to NADH at the physiological concentration (<100 μM NADH), but no notable response to other pyridine nucleotide was observed (FIGS. 5 and 6).

Example 7 Localization and Expression of Fluorescent Sensor for NADH in Different Subcellular Organelles

The NADH fluorescence sensor gene (Frex) was obtained using pRSET_(b)-ydiH-cpYFP-ydiH(D2) as template, and double-digesting it with BamHI and HindIII. The digested fragment was recovered and ligated to the following vectors: pcDNA3.1-Hygro-Cyto, pcDNA3.1-Hygro-Mito, pcDNA3.1-Hygro-Nuc, pcDNA3.1-Hygro-Mem, pcDNA3.1-Hygro-Golgi, pcDNA3.1-Hygro-ER and pcDNA3.1-Hygro-Peroxi respectively (engineered in Protein Chemistry Laboratory of East China University of Science and Technology, Shanghai, China).

Preparation: unless otherwise indicated, all primers used herein were synthesized by Shanghai Sangon (Sangon Biotech (Shanghai Co. Ltd., Shanghai, China). First, vector pcDNA3.1-Hygro-Cyto was constructed based on pcDNA3.1-Hygro (+) (Invitrogen, California, U.S.A.). Two primers: Cyto Forward Primer and Cyto Reverse Primer, were designed.

Cyto Forward Primer: (SEQ ID No 80) CTAGC ATGGC GGATCC ACTAGT AAGCTT AAG C Cyto Reverse Primer: (SEQ ID No 81) TCGAG CTT AAGCTT ACTAGT GGATCC GCCAT G

This primer pair contains restriction sites and the start codon ATG, and the structure was “NheI-ATG-GC-BamHI-HindIII-XhoI”. Following steps for dual primer annealing with the obtained primers was carried out.

-   -   1. The primer powder was dissolved to 100 μM in specific buffer         (10 mM Tris, pH7.5-8.0; 50 mM NaCl, 1 mM EDTA).     -   2. Equimolar amounts of the primer pair to be annealed were         mixed to a total volume of no greater than 500 μl.     -   3. The mixture was heated to 95° C. and then slowly cooled to         room temperature (below 30° C.), then stored at −20° C. before         use.

For organelle targeting signal Mito (SEQ ID No 82) and Golgi (SEQ ID No 83), the signal was introduced into vector pcDNA3.1-Hygro(+) through double-digestion utilizing synthesized targeting signal containing NheI restriction site allocated at 5′ end and BamHI restriction site allocated at 3′ end.

Double-digestion system DNA fragment 10 μl NheI  1 μl BamHI  1 μl 10x Tangobuffer  5 μl ddH₂O 33 μl Total 50 μl

Double-digestion system Vector:pcDNA3.1-Hygro(+) 10 μl NheI  1 μl BamHI  1 μl 10x Tangobuffer  5 μl ddH₂O 33 μl Total 50 μl

Similarly, for organelle targeting signal Nuc, Mem, ER and Peroxi, a pair of restriction sites were allocated to their both ends, respectively. Synthesized primers were utilized in dual primer annealing for the formation of double-stranded DNA, double-stranded DNA fragment with sticky ends obtained directly thereby was subsequently ligated with double-digested vector pcDNA3.1-Hygro(+).

Nuc Forward Primer: (SEQ ID No 84) AGCTT GATCCAAAAAAGAAGAGAAAGGTAGATCCAAAAAAGAAGAGA AAGGTAGATCCAAAAAAGAAGAGAAAGGTAG C Nuc Reverse Primer: (SEQ ID No 85) TCGAG CTACCTTTCTCTTCTTTTTTGGATCTACCTTTCTCTTCTTTTTT GGATCTACCTTTCTCTTCTTTTTTGGATC A Mem Forward Primer: (SEQ ID No 86) CTAGC ATGGCGCTGTGCTGTATGAGAAGAACCAAACAGGTTGAAAAG AATGATGAGGACCAAAAGATCGC G Mem Reverse Primer: (SEQ ID No 87) GATCC GCGATCTTTTGGTCCTCATCATTCTTTTCAACCTGTTTGGTTCT TCTCATACAGCACAGCGCCAT G ER Forward Primer: (SEQ ID No 88) CTAGC ATGGCGCTGCTATCCGTGCCGTTGCTGCTCGGCCTCCTCGG CCTGGCCGTCGCCGC G ER Reverse Primer: (SEQ ID No 89) GATCC GCGGCGACGGCCAGGCCGAGGAGGCCGAGCAGCAACGGCAC GGATAGCAGCGCCAT G Peroxi Forward Primer:  (SEQ ID No 90) AGCTT TCCAAGCTGTAA C Peroxi Reverse Primer:  (SEQ ID No 91) TCGAG TTACAGCTTGGA A

Recombinant plasmids pcDNA3.1-Hygro-Cyto-Frex, pcDNA3.1-Hygro-mito-Frex, pcDNA3.1-Hygro-Frex-Nuc, pcDNA3.1-Hygro-mem-Frex, pcDNA3.1-Hygro-golgi-Frex, pcDNA3.1-Hygro-Frex-ER and pcDNA3.1-Hygro-Frex-peroxi were constructed, and then sequenced. The results demonstrated that the nucleotide sequences of Frex fragment were the same as SEQ ID NO: 9. HEK293 cells, HEK293FT cells and Cos7 cells were transfected with these recombinant plasmids, respectively. The transfected cells were observed under a laser scanning confocal microscope (Nikon, Japan) with two excitation wavelengths at 405 nm and 488 nm, while the emission wavelength was 500-550 nm.

Experimental results indicated that, in HEK293FT cells, Frex-Cyto was efficiently and accurately located in the cytoplasm (FIG. 7A); Frex-Mito was efficiently and accurately located in the mitochondria (FIG. 7B); Frex-Nuc was efficiently and accurately located in the nucleus (FIG. 7C); Frex-Mem was efficiently and accurately located in the membrane (FIG. 7D); Frex-Golgi was efficiently and accurately located in the Glogi (FIG. 7E); Frex-ER was efficiently and accurately located in the endoplasmic reticulum (FIG. 7F); Frex-Pero was efficiently and accurately located in the peroxisomes (FIG. 7G).

Example 8 Utilizing the Sensor Series to Indicate Changes of Intracellular Reduced Nicotinamide Adenine Dinucleotide

(1) Fluorescent sensors for reduced nicotinamide adenine dinucleotide used in real-time measurements of increases of NADH levels in different subcellular compartments as the result of trans-membrane entrance of NADH into the cell.

As described in Example 7, the fluorescence sensors for reduced nicotinamide adenine dinucleotide were expressed in different subcellular organelles of 293FT cells. Results showed that this series of sensors are capable of detecting, in real time, the changes in intracellular NADH levels upon the addition of external NADH in cell culture medium (FIG. 8-1A). Following the addition of external NADH into cell culture medium, transfected cells were observed under a laser scanning confocal microscope (Nikon, Japan). The results indicated that, the emission fluorescence at 528 nm upon 485 nm excitation of the sensor was 2.5 times stronger than that of the control group, proving NADH could enter cells across the membrane and lead to the immediate increase of intracellular NADH levels; FIG. 8-1D and FIG. 8-1E showed that the fluorescence sensor for reduced nicotinamide adenine dinucleotide was not interfered by NADH analogs such as NAD⁺, NADPH, etc. As to the control group in comparison, the cpYFP presented alone was not affected by extra NADH either. Therefore, effects of pH and the variation in cpYFP per se by environmental changes could be excluded. This series of sensors were further utilized to detect influences of extra NADH on other organelles, and observed that extra NADH could also increase the NADH levels in nucleus and mitochondria, the results for nucleus study are shown in FIG. 8-1B, and those for mitochondria study are shown in FIG. 8-1C. In conclusion, our results indicated that fluorescent sensors for nicotinamide adenine dinucleotide could serve as a good gauge for the increase of NADH levels in mammalian cells upon the transmembrane entrance of NADH.

(2) Fluorescent sensor for nicotinamide adenine dinucleotide used in real-time measurements of NADH levels in different subcellular compartments regulated by glucose, pyruvate and lactate.

Glycolysis is an important pathway of producing NADH and it plays a vital role in regulating intracellular NADH levels. The nicotinamide adenine dinucleotide fluorescent sensors were used to test how several important metabolites in this pathway, glucose, pyruvate and lactate, would influence the NADH levels in different subcellular compartments. FIG. 8-2A shows results within cytoplasm and FIG. 8-2D shows results within mitochondria. These results indicated that, as one source of cellular energy, glucose could lead to the increase the cytoplasmic and mitochondrial levels of NADH. As products of glycolysis pathway, pyruvate and lactate are presented in the cytoplasm with a dynamic balance between them. At increased intracellular levels of pyruvate, lactate dehydrogenase consumes NADH and produces lactate and NAD⁺, and in turn, leads to the decrease of NADH levels in cytoplasm. At increased intracellular levels of lactate, lactate dehydrogenase consumes NAD⁺ and produces pyruvate and NADH, and in turn, leads to the increase of NADH levels in cytoplasm. FIG. 8-2B shows that pyruvate could cause a rapid decline of NADH levels in cytoplasm, but it resumed to normal levels over time. FIG. 8-2C shows that lactate could cause a rapid increase of NADH levels in cytoplasm, but also resumed to normal levels over time. In conclusion, these results demonstrated that the fluorescence sensors for nicotinamide adenine dinucleotide could monitor, in real-time, the regulated dynamic balance of NADH levels in cytoplasm.

(3) Fluorescent sensors for reduced nicotinamide adenine dinucleotide used in real-time detection of NADH levels in mitochondria regulated by oxidative phosphorylation pathway.

NADH that produced via glycolysis pathway and tricarboxylic acid cycle pathway will be oxidized by the oxidative phosphorylation pathway of mitochondrial respiratory chain, and then generate ATP to provide energy for various life activities. Fluorescent sensors for nicotinamide adenine dinucleotide were used to measure changes of NADH levels in mitochondria when various complexes in the respiratory chain were inhibited. FIG. 8-3A shows a 6-minute dynamic profile of the NADH sensor, which was expressed in mitochondria, upon 3-NP treatment. FIG. 8-3B shows a 6-minute dynamic profile of the control protein cpYFP, which was expressed in mitochondria, upon 3-NP treatment. Time interval between the figures was 1 min. The cells were observed before and after treatment under a laser scanning confocal microscope (Nikon, Japan). Results showed that, complex II inhibitor 3-NP caused a greatly decline of NADH levels in mitochondrial because of inhibited TCA cycle, whereas in the control group, cpYFP showed no obvious change. FIG. 8-3C shows the measurement of the effect of other complex inhibitors on NADH levels in mitochondria using fluorescent sensor for nicotinamide adenine dinucleotide. Results showed that, upon treated with complex I inhibitor rotenone, complex III inhibitor antimycin A, and complex IV inhibitor NaCN, respectively, for 30 min, the fluorescence (ex 485, em 528) of the sensor was increased, indicating that these inhibitors prevented the oxidation of NADH by inhibiting oxidative phosphorylation pathway, thus, led to the increase of NADH levels in mitochondria (FIG. 8-3C).

Example 9 Measurement of Changes in Intracellular NAD⁺ Level by Fluorescent Sensors for Oxidized Nicotinamide Adenine Dinucleotide

Fluorescent sensor for oxidized nicotinamideadenine dinucleotide has a structure with cpYFP inserted into Trex between two amino acids, F189 and L190. The sequence of said sensor is SEQ ID NO: 129. Said sensor was prepared as described in Example 4. By expressing said sensors in cytoplasm of 293FT cells, we found that real-time monitor of the effects on intracellular NAD levels of adding NAD⁺ into cell culture medium could be well achieved using this series of sensors (FIG. 9-1). As shown in FIG. 9-1, upon the addition of external NAD⁺ into cell culture medium, the fluorescence of 528 nm emission upon 485 nm excitation was rapidly enhanced by about 2.8 times, proving that fluorescence sensor for oxidized nicotinamide adenine dinucleotide is a good gauge for the increase of NAD⁺ levels in mammalian cells upon the transmembrane entrance of NAD⁺. In protein detection with single channel 485 nm excitation and 528 nm emission, Frex-2 sensors responded to NAD⁺ by about 1000% (FIG. 9-2), while they exhibited no response to NADP, NADPH, ADP and ATP (FIG. 9-3).

Example 10 Measurement of Changes in NADH/NAD⁺ Ratio by Fluorescent Sensors for Reduced/Oxidized Nicotinamide Adenine Dinucleotide Ratio

Fluorescent sensor for reduced/oxidized nicotinamide adenine dinucleotide ratio has a structure with cpYFP inserted into Trex between two amino acids, F189 and L190. The sequence of said sensor is SEQ ID NO: 148. Said sensor was prepared as described in Example 4. Said sensor exhibited response only to NADH and NAD⁺, but no response to NADH analogs. Upon 485 nm excitation, binding with NADH and NAD⁺ could both lead increased fluorescence emission at 528 nm. However, upon 420 nm excitation, said sensor could only respond to NADH binding. Since 420 nm and 485 nm excitation could both produce emission fluorescence at 528 nm, different excitation wavelengths could be used to measure the ratio of fluorescence intensity emitted at 528 nm (420 nm/485 nm), it has been found that NADH binding increases the response in said fluorescence ratio, while NAD⁺ binding decreases the response in said fluorescence ratio (FIG. 10-1). This pattern is more evident when the total concentration of NADH and NAD⁺ remained unchanged, but would not change with the total concentration per se (FIG. 10-2).

At the presence of 20 uM NADP, NADPH, ADP and ATP, titration of [NADH]/[NAD⁺] at indicated ratio was conducted, we could find the responsive value and variation pattern were not affected, indicating that NADP, NADPH, ADP and ATP have no effect on the sensor (FIG. 10-3).

Therefore, said sensor could be used not only as a sensor for reduced/oxidized nicotinamide adenine dinucleotide ratio but also a sensor for reduced nicotinamide adenine dinucleotide alone.

Example 11 High-Throughput Drug Screening Based on Fluorescence Sensor for Reduced/Oxidized Nicotinamide Adenine Dinucleotide Ratio

It is generally believed that there is a dynamic balance between the concentration of pyruvate and lactate in cytoplasm and the concentration of free NADH and NAD⁺ in cytoplasm. In healthy tissues, pyruvate produced by glycolysis mainly enters mitochondria to participate TCA cycle and eventually generates a large amount of energy through oxidative phosphorylation. But in malignant tissues, pyruvate is mainly reduced to lactate by lactate dehydrogenase, accompanied by oxidizing NADH to NAD⁺. We developed a new method of high-throughput drug screening based the metabolic variation using superFrex, a fluorescent sensor for reduced/oxidized nicotinamide adenine dinucleotide ratio.

Stable cell lines expressing superFrex were mixed with different agents, then loaded into a black 384-well plate, and the fluorescence of superFrex was measured with a Multifunctional Microplate Reader (FIG. 11-A). For instance, from Merck's Protein kinase inhibitor compound library, we discovered 23-26 compounds increasing the ratio of intracellular lactate/pyruvate, and 7-9 compounds reducing the ratio of intracellular lactate/pyruvate (FIG. 11-B, 11-C). By further analyzing these compounds for the effect on the proliferation of normal cells and tumor cells, several lead compounds were eventually identified. These lead compounds could, at a certain dose range, effectively kill tumor cells but exhibited no toxicity to normal cells, therefore, has the potential to be developed as anticancer drugs.

Example 12 Measurement of NADH Metabolism in Tumor Cells Using Fluorescent Sensor for Reduced/Oxidized Nicotinamide Adenine Dinucleotide Ratio

H1299 tumor cells were transfected with pcDNA3.1-cyt-superFrex, and then screened under Hygromycin B for 2 weeks. Single clones of H1299 stable cell lines that exhibiting robuse expression of superFrex were obtained by flow cytometry sorting (H1299-superFrex). Male nude mice of 5-6 weeks old were subcutaneously injected with 200 μl of H1299-superFrex cell suspension (1.0×10⁷ cells) into their right armpits and housed for 3-4 weeks at SPF Animal facility, tumors in the nude mice grew to 0.6-1.0 cm. The nude mice were anaesthetized and then injected with 300 μl of sodium pyruvate (100 mM) via the tail vein. Effects of the agent on tumor metabolism were observed immediately with Kodak multifunctional vivo imaging system (Carestream, USA). Experimental results showed that, pyruvate resulted a quick decrease in the fluorescence of 420 nm channel of superFrex in tumor tissues, and a quick increase in the fluorescence of 490 nm channel of superFrex, leading to a decrease in ratio 420/490 nm (FIG. 12-A). As the experimental control, tumor cells expressing cpYFP exhibited no difference caused thereby (FIG. 12-B), indicating pyruvate caused the decrease of NADH/NAD⁺ ratios in tumor cells. Over time, pyruvate was gradually consumed metabolically, and the ratio of NADH/NAD⁺ in tumor cells resumed the initial level (FIG. 12-C). In summary, superFrex, the fluorescent sensor for reduced/oxidized nicotinamide adenine dinucleotide ratio, works well in real-time monitoring of the NADH metabolism in tumor tissues.

Other Embodiments

A number of embodiments are described herein. However, it should be understood that, in view of this specification, variations and modifications will be apparent to those skilled in the art, without departing from the spirit and scope of the invention. Therefore, these alternative embodiments are also included within the scope of the appended claims. 

What is claimed is:
 1. A genetically encoded fluorescent sensor for NADH, said fluorescent sensor being a fusion protein comprising (a) a polypeptide sensitive to environmental NADH, and (b) a segment that exhibits the environmental NADH by change in its spectral characteristics, wherein the polypeptide sensitive to NADH is: (1) a polypeptide derived from ydiH, a bacterial transcription factor Rex protein, wherein the polypeptide is encoded by a sequence selected from SEQ ID NO: 1 or 3; (2) a homologous or non-homologous sequence that is 95% identical to the sequence of (1); or (3) a homologous or non-homologous sequence that is 90% identical to the sequence of (1); a NADH binding fragment or NADH binding domain thereof; and wherein the segment that exhibits the environmental NADH by change in the spectral characteristic is a fluorescent protein sequence or a derivative thereof and is inserted between residue 189 and residue 190 of the polypeptide encoded by SEQ ID NO: 1 or between full length of the polypeptide encoded by SEQ ID NO: 3 and residues 85-215 of the polypeptide encoded by SEQ ID NO:
 3. 2. The fluorescent sensor for NADH according to claim 1, wherein the fluorescent sensor comprises: (1) an amino acid sequence selected from the group consisting of SEQ ID NO: 4, 5, 6, 7, and 8; (2) a homologous or non-homologous sequence that is 95% identical to the sequence of (1); or (3) a homologous or non-homologous sequence that is 90% identical to the sequence of (1).
 3. The fluorescent sensor according to claim 1, wherein the fluorescent sensor further comprises specific subcellular localization signal, wherein the localization signal allows localization of a target protein into a specified subcellular organelle.
 4. A kit for detection of NADH, drug screening or disease diagnosis, comprising the fluorescent sensor according to claim
 1. 